AIROS 8 Sequential Compression Device— 510(k) K172779
Substantially EquivalentAiros Medical, Inc.
FDA 510(k) clearance K172779 for AIROS 8 Sequential Compression Device, Substantially Equivalent on 2018-06-22. Applicant: Airos Medical, Inc..
Clearance details
- Applicant
- Airos Medical, Inc.
- Product code
- Code JOW
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Audubon, PA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.