510(k) K980508 ยท HNO Keratome, Ac-Powered
KERATOME BLADE, CHIROM MODEL ALK 500500; KERATOME BLADE, S.C.M.D. MODEL TUROKERATOME 400400
| Applicant | Micro Specialties, Inc., Milford CT, US |
| Decision | Substantially Equivalent, May 1, 1998 |
| Received | Feb 10, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980508
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.