510(k) K021640 ยท HNO Keratome, Ac-Powered
HANSATOME EXCELLUS MICROKERATOME
| Applicant | Bausch & Lomb, Inc., St. Louis MO, US |
| Decision | Substantially Equivalent, Jun 19, 2002 |
| Received | May 20, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021640
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.