510(k) K913697 ยท HNO Keratome, Ac-Powered
AUTOMATIC CORNEAL SHAPER
| Applicant | Hansa Research & Development, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Nov 5, 1991 |
| Received | Aug 19, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913697
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.