Omp Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cuff Pacer Ref K780703
Regimes: 510(k) Registry: 510(k)Syringe Set, 3-Way Thermodilutin Ref K760402
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Omp Laboratories, Inc. have in the registry?
The registry currently lists 2 devices for Omp Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Omp Laboratories, Inc.'s devices?
Among its 2 most recently registered devices, Omp Laboratories, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Omp Laboratories, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Omp Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Omp Laboratories, Inc. in the registry?
The most recently registered devices listed for Omp Laboratories, Inc. include CUFF PACER and SYRINGE SET, 3-WAY THERMODILUTIN.