Path Medical GmbH
FDA Regulatory Profile
Path Medical GmbH appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 3, 2022.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K220139 | QScreen | August 3, 2022 |
| K213345 | Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced, NavPRO ONE | June 22, 2022 |
| K211147 | ALGO 7i | October 14, 2021 |
| K133012 | SENTIERO | June 9, 2014 |
| K131141 | EARPROBE | June 27, 2013 |
| K100661 | EARPROBE | July 1, 2010 |