Data / Medical devices / United States / Medi Nuclear Corp., Inc.
Medi Nuclear Corp., Inc.: FDA-registered device maker in Baldwin Park, CA, United States, 6 510(k) clearances
Medi Nuclear Corp., Inc. is registered with the FDA (registration 2050098) in Baldwin Park, CA, United States. It lists 3 device types. The FDA files 6 510(k) clearances under its listings, the newest dated November 26, 2008. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2050098
- Address
- 4610 Littlejohn ST., Baldwin Park, CA, United States, 91706
- Owner or operator
- MEDI NUCLEAR CORPORATION INC. (2050098)
- Roles
- Manufacturer
- First device listed
- October 23, 1992
- Registered through
- 2026
- Brand names listed
- ARK Cart, with 2 E Tank Holders ARK-10E, Cart Metal ARK-10M, NEB-90 Large Volume Medication Nebulizer, Aero/Vent Jr Aerosol Unit AV-100H with Accessories AV-100HM, AV-100HS, AV-100HV, Shield AV-101A, Aero/Vent Plus Aerosol Unit AV-400+ Access AV-400+M,AV-400+S,AV-400+V, Aero/Vent Max AV-500, AV-500M, Shield AV-501A, Asthma Rescue Kit - ARK-1, ARK-3, ARK-5, ARK-7, ARK-21, ARK-23, ARK-25, ARK-27, HEALTHLINE MEDICATOR / REDINEB AEROSOL DRUG DELIVERY SYSTEM MR-502HB, MR502HH, MR-902HB, MR902HH, Insta/Vent & Insta/Vent Plus with Accessories IV-600M, IV-600PM, IV-600S, IV-600V, Insta/Vent ACCESSORIES MN1200, MN1212, MN1213, MN4046, MN0304, MN0305, MN2550B, MN8040, MN8050, IV-608A, MN1690, Insta/Vent Delivery Unit Shield - IV-601A and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Mouthpiece, Breathing | BYP | 1 | Manufacturer | accessdata.fda.gov |
| Nebulizer (Direct Patient Interface) | CAF | 2 | Manufacturer | accessdata.fda.gov |
| System, Rebreathing, Radionuclide | IYT | 2 | Manufacturer | accessdata.fda.gov |
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 |
|---|---|---|---|---|---|---|
| November 26, 2008 | K082541 | HEALTHLINE MEDICATOR / REDINEB AEROSOL DRUG DELIVERY SYSTEM | CAF | Substantially Equivalent | Medi Nuclear Corp., Inc. | accessdata.fda.gov |
| June 30, 2008 | K080657 | NEB-90 LARGE VOLUME MEDICATION NEBULIZER | CAF | Substantially Equivalent | Medi Nuclear Corp., Inc. | accessdata.fda.gov |
| April 26, 1996 | K960397 | MEDICATOR AEROSOL DRUG DELIVERY SYSTEM | CAF | Substantially Equivalent | Healthline Medical | accessdata.fda.gov |
| October 20, 1987 | K865107 | AERO-VENT AEROSOL UNIT | IYT | Substantially Equivalent | Medi Nuclear Corp., Inc. | accessdata.fda.gov |
| January 15, 1987 | K865093 | SAFE-T-SHIELD MOUTHPIECE | BYP | Substantially Equivalent | Medi Nuclear Corp., Inc. | accessdata.fda.gov |
| April 14, 1981 | K810819 | MEDI/NUCLEAR #XE-102 XENON/MASTER | IYT | Substantially Equivalent | Medi Nuclear Corp., Inc. | accessdata.fda.gov |
Compare with other makers
- All makers of System, Rebreathing, Radionuclide
- All makers of Nebulizer (Direct Patient Interface)
- All makers of Mouthpiece, Breathing
Updated November 26, 2008. 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.