Angiolaz, Inc.
United StatesFDA applicant, unverified
- Devices
- 10
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Ves 3001/2 Dual Output Video Illuminator Ref K981821
Regimes: 510(k) Registry: 510(k)Ves 3001-M Complete Video Endoscopic System Ref K982397
Regimes: 510(k) Registry: 510(k)Angiolaz Angioscope Catheter Ref K913129
Regimes: 510(k) Registry: 510(k)Ves 1501-M Ref K982409
Regimes: 510(k) Registry: 510(k)50 W Metal Halide Illuminator, Ves 0501. Ref K992447
Regimes: 510(k) Registry: 510(k)Headlamp HL2000. Ref K994362
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Angiolaz Ves-1CAM Ref K981819
Regimes: 510(k) Registry: 510(k)Ultra-Vu Angioscope Ref K902329
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Angiolaz, Inc. have in the registry?
The registry currently lists 10 devices for Angiolaz, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Angiolaz, Inc.'s devices?
Among its 10 most recently registered devices, Angiolaz, Inc. has devices listed in FDA 510(k) (10 devices).
What risk classes do Angiolaz, Inc.'s devices fall under?
Among its 10 most recently registered devices, the classes recorded for Angiolaz, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Angiolaz, Inc. in the registry?
The most recently registered devices listed for Angiolaz, Inc. include VES 3001/2 DUAL OUTPUT VIDEO ILLUMINATOR, VES 3001-M COMPLETE VIDEO ENDOSCOPIC SYSTEM, ANGIOLAZ ANGIOSCOPE CATHETER and VES 1501-M.