Data / Medical devices / United States / Netech Corp.
Netech Corp.: FDA-registered device maker in E Farmingdale, NY, United States, 2 510(k) clearances
Netech Corp. is registered with the FDA (registration 2436826) in E Farmingdale, NY, United States. It lists 7 device types. The FDA files 2 510(k) clearances under its listings, the newest dated November 8, 1996. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2436826
- FEI number
- 1000522032
- Address
- 110 Toledo ST., E Farmingdale, NY, United States, 11735
- Owner or operator
- NETECH CORPORATION (9021637)
- Roles
- Manufacturer
- First device listed
- September 15, 1995
- Registered through
- 2026
- Brand names listed
- Delta 1600, Delta 3300, Digiflow 2000, Digimano 1000, Digimano 2000, Digimano 2500, EXPMT 2000, LKG 601 and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Alarm, Leakage Current, Portable | DSM | 1 | Manufacturer | accessdata.fda.gov |
| Analyzer, Pacemaker Generator Function | DTC | 2 | Manufacturer | accessdata.fda.gov |
| Flowmeter, Calibration, Gas | BXY | 1 | Manufacturer | accessdata.fda.gov |
| Gauge, Measuring | JYJ | 1 | Manufacturer | accessdata.fda.gov |
| Generator, Electroencephalograph Test Signal | GWR | 1 | Manufacturer | accessdata.fda.gov |
| Tester, Defibrillator | DRL | 2 | Manufacturer | accessdata.fda.gov |
| Tester, Electrode/Lead, Electroencephalograph | GYA | 1 | 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 8, 1996 | K961582 | EXTERNAL PACEMAKER ANALYZER, MODEL PMT 100 | DTC | Substantially Equivalent | North American Technical Services Corp. | accessdata.fda.gov |
| October 29, 1996 | K961595 | DEFIBRILLATOR ANALYZER, DELTA 1000 | DRL | Substantially Equivalent | Netech Corp. | accessdata.fda.gov |
Compare with other makers
- All makers of Tester, Electrode/Lead, Electroencephalograph
- All makers of Gauge, Measuring
- All makers of Analyzer, Pacemaker Generator Function
- All makers of Generator, Electroencephalograph Test Signal
- All makers of Tester, Defibrillator
Updated November 8, 1996. 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.