510(k) K921167 ยท GDX Scalpel, One-Piece
ULTRABLADE
| Applicant | Micron Technology, Inc., Boulder CO, US |
| Decision | Substantially Equivalent, Jul 30, 1992 |
| Received | Mar 11, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K921167
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.