Steri-Aid, Inc.
CanadaFDA applicant, unverified
- Devices
- 1
What Steri-Aid, Inc. makes
Steri-Aid, Inc. produces sterile barrier kits designed for single-use medical procedures, ensuring contamination control in clinical settings.
The company’s products are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Steri-Aid Kit Ref K963049
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Steri-Aid, Inc. have in the registry?
The registry currently lists 1 device for Steri-Aid, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Steri-Aid, Inc.'s devices?
Among its 1 most recently registered device, Steri-Aid, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Steri-Aid, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Steri-Aid, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Steri-Aid, Inc. in the registry?
The most recently registered devices listed for Steri-Aid, Inc. include STERI-AID KIT.