Webster Laboratories, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Electrode Catheter, Orthogonal Type Ref K841802
Regimes: 510(k) Registry: 510(k)Switching Unit Electrode Catheters Ref K823361
Regimes: 510(k) Registry: 510(k)Temperature Probes Ref K813271
Regimes: 510(k) Registry: 510(k)Switching Unit Electrode Catheter Ref K834602
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Webster Laboratories, Inc. have in the registry?
The registry currently lists 5 devices for Webster Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Webster Laboratories, Inc.'s devices?
Among its 5 most recently registered devices, Webster Laboratories, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Webster Laboratories, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Webster 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 Webster Laboratories, Inc. in the registry?
The most recently registered devices listed for Webster Laboratories, Inc. include CARDIOVASCULAR, THERMODILUTION, FLOW, CORONARY SIN, ELECTRODE CATHETER, ORTHOGONAL TYPE, SWITCHING UNIT ELECTRODE CATHETERS and TEMPERATURE PROBES.