Company ยท DE
Path Medical GmbH
FDA 510(k) clearances and medical device recalls filed under this name, 2010 to 2022. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Aug 3, 2022 | K220139 | QScreen Path Medical GmbH, DE | GWJ |
| Jun 22, 2022 | K213345 | Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced, NavPRO ONE Path Medical GmbH, DE | EWO |
| Oct 14, 2021 | K211147 | ALGO 7i Path Medical GmbH, DE | GWJ |
| Jun 9, 2014 | K133012 | SENTIERO Path Medical GmbH, DE | EWO |
| Jun 27, 2013 | K131141 | EARPROBE Path Medical GmbH, DE | GWJ |
| Jul 1, 2010 | K100661 | EARPROBE Path Medical GmbH | GWJ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||