510(k) K984540 ยท HNO Keratome, Ac-Powered
KERAVISION VACUUM RING SYSTEM
| Applicant | Keravision, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Apr 28, 1999 |
| Received | Dec 21, 1998 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K984540
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.