510(k) K980675 ยท HNO Keratome, Ac-Powered
SUMMIT KRUMEICH-BARRAQUER MICROKERATOME
| Applicant | Summit Technology, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Dec 22, 1998 |
| Received | Feb 20, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980675
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 6, 2003 | Alcon Laboratories, Inc SKBM Microkeratome cutting tool Terminated |
HNO | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.