Life-Line Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Endotracheal Tube Ref K821243
Regimes: 510(k) Registry: 510(k)Endotracheal Tube Ref K781339
Regimes: 510(k) Registry: 510(k)Endotracheal Tube Ref K821456
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Life-Line Products, Inc. have in the registry?
The registry currently lists 3 devices for Life-Line Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Life-Line Products, Inc.'s devices?
Among its 3 most recently registered devices, Life-Line Products, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Life-Line Products, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Life-Line Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Life-Line Products, Inc. in the registry?
The most recently registered devices listed for Life-Line Products, Inc. include ENDOTRACHEAL TUBE.