Deproco, Inc.
Country not established
- Devices
- 1
What Deproco, Inc. makes
Deproco, Inc. manufactures the Doctor Vellette’s Injector, a device designed for precise subcutaneous or intramuscular injections.
The company’s portfolio is regulated under FDA Class II devices and is listed via 510(k) clearance. The manufacturer is based in the United States.
Catalogue
Doctor Vellette's Injector Ref K833426
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Deproco, Inc. have in the registry?
The registry currently lists 1 device for Deproco, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Deproco, Inc.'s devices?
Among its 1 most recently registered device, Deproco, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Deproco, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Deproco, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Deproco, Inc. in the registry?
The most recently registered devices listed for Deproco, Inc. include DOCTOR VELLETTE'S INJECTOR.