Bio-Flow, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Bio-Flow, Inc. makes
Bio-Flow, Inc. manufactures urine flow measuring devices, including the QRI-FLOW and the Modified Bio-Flow Model 200, designed to assess urinary flow rates in clinical settings.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Qri-Flow Urine Flow Measuring Device Ref K851266
Regimes: 510(k) Registry: 510(k)Modified Bio-Flow Model 200 Urine Flow Device Ref K862251
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bio-Flow, Inc. have in the registry?
The registry currently lists 2 devices for Bio-Flow, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bio-Flow, Inc.'s devices?
Among its 2 most recently registered devices, Bio-Flow, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Bio-Flow, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Bio-Flow, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bio-Flow, Inc. in the registry?
The most recently registered devices listed for Bio-Flow, Inc. include QRI-FLOW URINE FLOW MEASURING DEVICE and MODIFIED BIO-FLOW MODEL 200 URINE FLOW DEVICE.