510(k) K023092 ยท HMY Keratome, Battery-Powered
BD K-4000 MICROKERATOME SYSTEM
| Applicant | Becton, Dickinson & CO, Franklin Lakes NJ, US |
| Decision | Substantially Equivalent, Oct 18, 2002 |
| Received | Sep 18, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023092
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 23, 2007 | Becton Dickinson and Company BD Microkeratome K3000 and K4000;Catalog Number: 378660, Becton Dickinson & Company (BD) Terminated |
HMY | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.