510(k) K983317 ยท HNO Keratome, Ac-Powered
BARRON MICROKERATOME SYSTEM, MODEL B2000
| Applicant | Barron Precision Instruments, LLC, Grand Blanc MI, US |
| Decision | Substantially Equivalent, Dec 2, 1998 |
| Received | Sep 21, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983317
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.