Bioscan, Inc.
United StatesFDA applicant, unverified
- Devices
- 9
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Q.P. Preamplifier Sys Ref K841683
Regimes: 510(k) Registry: 510(k)Eeg Analyzer Ref K925735
Regimes: 510(k) Registry: 510(k)Bio/Scan Biolog Cassette Recorder Ref K841684
Regimes: 510(k) Registry: 510(k)Eeg Electrodes Ref K841685
Regimes: 510(k) Registry: 510(k)Spinal Pad Ref K993684
Regimes: 510(k) Registry: 510(k)Bio-Log 8+1 Ambulatory Physiologic Recorder Ref K864928
Regimes: 510(k) Registry: 510(k)Biofind Ref K003480
Regimes: 510(k) Registry: 510(k)Light Patch Ref K993686
Regimes: 510(k) Registry: 510(k)Biopack Ref K993685
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bioscan, Inc. have in the registry?
The registry currently lists 9 devices for Bioscan, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bioscan, Inc.'s devices?
Among its 9 most recently registered devices, Bioscan, Inc. has devices listed in FDA 510(k) (9 devices).
What risk classes do Bioscan, Inc.'s devices fall under?
Among its 9 most recently registered devices, the classes recorded for Bioscan, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bioscan, Inc. in the registry?
The most recently registered devices listed for Bioscan, Inc. include Q.P. PREAMPLIFIER SYS, EEG ANALYZER, BIO/SCAN BIOLOG CASSETTE RECORDER and EEG ELECTRODES.