510(k) K904505 ยท GDX Scalpel, One-Piece
CCI CORNEAL SCARIFIER
| Applicant | Buckman Co., Inc., Concord CA, US |
| Decision | Substantially Equivalent, Apr 23, 1991 |
| Received | Oct 2, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904505
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.