510(k) K082043 ยท HNO Keratome, Ac-Powered
CARRIAZO-PENDULAR MICROKERATOME
| Applicant | Schwind Eye-Tech-Solutions GmbH & Co. KG, Kleinostheim, DE |
| Decision | Substantially Equivalent, Aug 1, 2008 |
| Received | Jul 18, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082043
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.