510(k) K884862 ยท GES Blade, Scalpel
ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADE
| Applicant | Anchor Products Co., Addison IL, US |
| Decision | Substantially Equivalent, Dec 27, 1988 |
| Received | Nov 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884862
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.