Airos Medical, Inc.
Airos Medical, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on October 11, 2024.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K240499 | ARTAIRA Arterial Compression Device (AACD01) | October 11, 2024 |
| K223195 | AIROS 6P Sequential Compression Device | December 9, 2022 |
| K223193 | AIROS 8P Sequential Compression Device | December 9, 2022 |
| K193068 | AIROS 8 Sequential Compression Device | December 4, 2019 |
| K193069 | AIROS 6 Sequential Compression Device | December 4, 2019 |
| K172779 | AIROS 8 Sequential Compression Device | June 22, 2018 |
| K172770 | AIROS 6 Sequential Compression Device | June 22, 2018 |