Substance Abuse Specialties, Inc.
Country not established
- Devices
- 1
What Substance Abuse Specialties, Inc. makes
Substance Abuse Specialties, Inc. makes the SASI-DC1TS device.
The SASI-DC1TS is a Class I medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Sasi-DC1TS Ref K970580
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Substance Abuse Specialties, Inc. have in the registry?
The registry currently lists 1 device for Substance Abuse Specialties, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Substance Abuse Specialties, Inc.'s devices?
Among its 1 most recently registered device, Substance Abuse Specialties, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Substance Abuse Specialties, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Substance Abuse Specialties, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Substance Abuse Specialties, Inc. in the registry?
The most recently registered devices listed for Substance Abuse Specialties, Inc. include SASI-DC1TS.