Data / Medical devices / United States / Medline Industries (NAMIC Division) - Glen Falls
Medline Industries (NAMIC Division) - Glen Falls: FDA-registered device maker in Glens Falls, NY, United States, 22 510(k) clearances
Medline Industries (NAMIC Division) - Glen Falls is registered with the FDA (registration 3015910259) in Glens Falls, NY, United States. It lists 14 device types. The FDA files 22 510(k) clearances under its listings, the newest dated January 6, 2017. Registered through 2027. FDA data exported November 2, 2026.
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- FDA registration number
- 3015910259
- Address
- 10 Glen Falls Technical Park Drive, Glens Falls, NY, United States, 12801
- Owner or operator
- Medline Industries, LP (1417592)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- July 9, 2008
- Registered through
- 2027
- Brand names listed
- AVENUE Insertion Tool, Angio-SAC Collection System, Blazer Dx, CELSIUS, Carto 3 Interface Cable, Carto 3 System eco, Catheter Interface Cable, Easy - Mate and more
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| January 6, 2017 | K163141 | NAMIC ClearaCIL Contrast Injection Lines | DQO | Substantially Equivalent | AngioDynamics, Inc. | accessdata.fda.gov |
| April 14, 2014 | K140194 | NAMIC RCS SYRINGE | FMF | Substantially Equivalent | Navilyst Medical, Inc. | accessdata.fda.gov |
| November 28, 2011 | K113198 | NMI CONTROL SYRINGE, 7 ML NMI CONTROL SYRINGE, 8 ML | DXT | Substantially Equivalent | Navilyst Medical, Inc. | accessdata.fda.gov |
| March 25, 1996 | K951722 | PERCEPTOR COMPENSATOR MORSE MANIFOLD | DRS | Substantially Equivalent | Namic | accessdata.fda.gov |
| July 21, 1995 | K951802 | SCIMED ENCORE ADVANTAGE KIT AND THE ESSENTIALS KIT | DXT | Substantially Equivalent | Scimed Life Systems, Inc. | accessdata.fda.gov |
| December 10, 1992 | K922706 | SCIMED SIDELINER | DQX | Substantially Equivalent | Scimed | accessdata.fda.gov |
| July 23, 1992 | K922410 | SCIMED AVENUE CORONARY GUIDEWIRE INSERTION TOOL | DQX | Substantially Equivalent | Scimed Life Systems, Inc. | accessdata.fda.gov |
| April 22, 1991 | K910764 | THE PERCEPTOR(TM) STAND ALONE TRANSDUCER | DRS | Substantially Equivalent | North American Instrument Corp. | accessdata.fda.gov |
| March 26, 1991 | K903493 | NAMIC CONTRAST SAVINGS DELIVERY SYSTEM | IZI | Substantially Equivalent | North American Instrument Corp. | accessdata.fda.gov |
| September 27, 1990 | K903606 | GUIDEWIRE TORQUE DEVICE AND GUIDEWIRE INTRODUCER | LIT | Substantially Equivalent | North American Instrument Corp. | accessdata.fda.gov |
| August 23, 1990 | K902472 | MORSE DT MANIFOLD | DRS | Substantially Equivalent | North American Instrument Corp. | accessdata.fda.gov |
| June 26, 1990 | K900652 | NAMIC PTCA Y-ADAPTOR | DTL | Substantially Equivalent | North American Instrument Corp. | accessdata.fda.gov |
| January 9, 1990 | K896108 | THE PILOT SCIMED TORQUE DEVICE | LOX | Substantially Equivalent | Scimed Life Systems, Inc. | accessdata.fda.gov |
| January 12, 1989 | K884408 | NAMIC DUAL BACKCHECK VALVE | DTL | Substantially Equivalent | North American Instrument Corp. | accessdata.fda.gov |
| February 5, 1988 | K873955 | NAMIC ANGIOGRAPHIC SYRINGE | DXT | Substantially Equivalent | North American Instrument Corp. | accessdata.fda.gov |
| July 25, 1985 | K850898 | MEDI-TRACE DISPOSABLE PRESSURE TRANSDUCER | DRS | Substantially Equivalent | Medi-Trace Products Division | accessdata.fda.gov |
| May 30, 1985 | K852140 | NAMIC CONTRAST & FLUID DELIVERY SPIKES(VARIOUS) | FPA | Substantially Equivalent | North American Instrument Corp. | accessdata.fda.gov |
| October 18, 1984 | K843726 | NAMIC ADB ANGIOGRAPHIC DUMP BAG | DQO | Substantially Equivalent | North American Instrument Corp. | accessdata.fda.gov |
| October 18, 1984 | K842829 | HIGH PRESSURE, 1 & 3 WAY STERILE DISPOS | DTL | Substantially Equivalent | North American Instrument Corp. | accessdata.fda.gov |
| August 24, 1982 | K822100 | HIGH PRESSURE CONTRAST INJECTION LINE | DQO | Substantially Equivalent | Namic | accessdata.fda.gov |
| January 25, 1979 | K790082 | ARTERIAL EXTENSION SET | DQO | Substantially Equivalent | Namic | accessdata.fda.gov |
| January 23, 1979 | K782095 | STOPCOCKS, MANIFOLDS | DTL | Substantially Equivalent | Namic | accessdata.fda.gov |
Compare with other makers
- All makers of Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
- All makers of Angiography/Angioplasty Kit
- All makers of Transducer, Blood-Pressure, Extravascular
- All makers of Catheter, Intravascular, Diagnostic
- All makers of Cardiovascular Procedure Kit
- All makers of Injector And Syringe, Angiographic
Updated January 6, 2017. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.