Latex Medical Devices, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
O.N.A.T. Ref K812102
Regimes: 510(k) Registry: 510(k)O.N.A.T. Ref K820175
Regimes: 510(k) Registry: 510(k)Blood Pressure Cuff Ref K896986
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Latex Medical Devices, Inc. have in the registry?
The registry currently lists 3 devices for Latex Medical Devices, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Latex Medical Devices, Inc.'s devices?
Among its 3 most recently registered devices, Latex Medical Devices, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Latex Medical Devices, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Latex Medical Devices, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Latex Medical Devices, Inc. in the registry?
The most recently registered devices listed for Latex Medical Devices, Inc. include O.N.A.T. and BLOOD PRESSURE CUFF.