Dermatech Medical, Inc.
Country not established
- Devices
- 1
What Dermatech Medical, Inc. makes
Dermatech Medical, Inc. manufactures the Dermatech IV Holder, a device designed to secure intravenous lines and tubing to prevent dislodgement during patient care.
The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Dermatech Iv Holder Ref K060488
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dermatech Medical, Inc. have in the registry?
The registry currently lists 1 device for Dermatech Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dermatech Medical, Inc.'s devices?
Among its 1 most recently registered device, Dermatech Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Dermatech Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Dermatech Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dermatech Medical, Inc. in the registry?
The most recently registered devices listed for Dermatech Medical, Inc. include DERMATECH IV HOLDER.