Biomedical Research & Development Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Biomedical Research & Development Laboratories, Inc. makes
Biomedical Research & Development Laboratories, Inc. makes the Universal™ Ion Select Electrode Standards, H.P.T. Home Preg. Test Kit & A.P.T., and Spectrum™ Blood Gas and Electrolyte Control.
These devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Universal(Tm) Ion Select Electrode Standards Ref K884693
Regimes: 510(k) Registry: 510(k)H.P.T. Home Preg. Test Kit & A.P.T. Ref K834474
Regimes: 510(k) Registry: 510(k)Spectrum(Tm) Blood Gas And Electrolyte Control Ref K881655
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biomedical Research & Development Laboratories, Inc. have in the registry?
The registry currently lists 3 devices for Biomedical Research & Development Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biomedical Research & Development Laboratories, Inc.'s devices?
Among its 3 most recently registered devices, Biomedical Research & Development Laboratories, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Biomedical Research & Development Laboratories, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Biomedical Research & Development Laboratories, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biomedical Research & Development Laboratories, Inc. in the registry?
The most recently registered devices listed for Biomedical Research & Development Laboratories, Inc. include UNIVERSAL(TM) ION SELECT ELECTRODE STANDARDS, H.P.T. HOME PREG. TEST KIT & A.P.T. and SPECTRUM(TM) BLOOD GAS AND ELECTROLYTE CONTROL.