Metron U.S., Inc.
United StatesFDA applicant, unverified
- Devices
- 4
What Metron U.S., Inc. makes
Metron U.S., Inc. manufactures medical testing and simulation equipment, including defibrillator testers, I.V. pump testers, SpO2 analyzers, and patient simulators.
These Class II devices are listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Qa-40M Defibrillator Tester Ref K963190
Regimes: 510(k) Registry: 510(k)Metron Qa-Ids I.V. Pump Tester Ref K982020
Regimes: 510(k) Registry: 510(k)Metron Qa-510 SPO2 Analyzer Ref K973991
Regimes: 510(k) Registry: 510(k)Ps-41 6M Patient Simulator Ref K963198
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Metron U.S., Inc. have in the registry?
The registry currently lists 4 devices for Metron U.S., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Metron U.S., Inc.'s devices?
Among its 4 most recently registered devices, Metron U.S., Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do Metron U.S., Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for Metron U.S., Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Metron U.S., Inc. in the registry?
The most recently registered devices listed for Metron U.S., Inc. include QA-40M DEFIBRILLATOR TESTER, METRON QA-IDS I.V. PUMP TESTER, METRON QA-510 SPO2 ANALYZER and PS-41 6M PATIENT SIMULATOR.