Biosan Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Abnormal Urine Control Ref K833191
Regimes: 510(k) Registry: 510(k)Photron Neurovisual Stimulator(Modification) Ref K853812
Regimes: 510(k) Registry: 510(k)Normal Urine Control Ref K833192
Regimes: 510(k) Registry: 510(k)Bio-Rex 70 Resin 100-200 Mesh PH6.2 Ref K833319
Regimes: 510(k) Registry: 510(k)Bio-Science Laboratories T4 Reagent Ref K834023
Regimes: 510(k) Registry: 510(k)Normal Goat Serum Ref K833318
Regimes: 510(k) Registry: 510(k)Tobramycin Reagent Ref K832763
Regimes: 510(k) Registry: 510(k)Photron Visual Field Analyzer Ref K860642
Regimes: 510(k) Registry: 510(k)Radioimmunoassay, Thyroid Stimu. Hormone Ref K833193
Regimes: 510(k) Registry: 510(k)Amberlite CG50 Resin, 100-200 Mesh Ref K833320
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biosan Laboratories, Inc. have in the registry?
The registry currently lists 10 devices for Biosan Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biosan Laboratories, Inc.'s devices?
Among its 10 most recently registered devices, Biosan Laboratories, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Biosan Laboratories, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Biosan 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 Biosan Laboratories, Inc. in the registry?
The most recently registered devices listed for Biosan Laboratories, Inc. include ABNORMAL URINE CONTROL, PHOTRON NEUROVISUAL STIMULATOR(MODIFICATION), NORMAL URINE CONTROL and BIO-REX 70 RESIN 100-200 MESH PH6.2.