510(k) K022637 ยท HMY Keratome, Battery-Powered
BD-3000 MICROKERATOME SYSTEM, MODEL K-3000 MICROKERATOME
| Applicant | Becton, Dickinson & CO, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Oct 16, 2002 |
| Received | Aug 8, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022637
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 12, 2003 | BD Opthalmic Systems BD K-3000 Microkeratome Blade
REF 378607 Terminated |
HMY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.