Bipore, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Bipore Accuflex Percutaneous Sheath Introducer Ref K964814
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Biopore Balloon Dilation Catheter Ref K041293
Regimes: 510(k) Registry: 510(k)Bipore Balloon Dilatation Catheter Ref K961980
Regimes: 510(k) Registry: 510(k)Bipore Balloon Dilation Catheter Ref K073318
Regimes: 510(k) Registry: 510(k)Bipore Accuflex Percutaneous Sheath Introducer Ref K051513
Regimes: 510(k) Registry: 510(k)Bipore Balloon Dilatation Catheter Ref K973563
Regimes: 510(k) Registry: 510(k)Bipore Accuflex Percutaneous Sheath Introducer Ref K073434
Regimes: 510(k) Registry: 510(k)Bipore Balloon Dilatation Catheter Ref K983650
Regimes: 510(k) Registry: 510(k)Bipore O.2 Micron Hydrophobic Filter Assembly Ref K844625
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bipore, Inc. have in the registry?
The registry currently lists 10 devices for Bipore, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bipore, Inc.'s devices?
Among its 10 most recently registered devices, Bipore, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Bipore, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Bipore, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bipore, Inc. in the registry?
The most recently registered devices listed for Bipore, Inc. include BIPORE ACCUFLEX PERCUTANEOUS SHEATH INTRODUCER, O.2 MICRON INFECTION RESISTANT HYDROPHOBIC FILTER, BIOPORE BALLOON DILATION CATHETER and BIPORE BALLOON DILATATION CATHETER.