510(k) K873391 ยท GDY Gauze/Sponge, Internal, X-Ray Detectable
MODIFIED ROUND (BEEHIVE) DISSECTOR 3/8
| Applicant | Ormed Mfg., Inc., Buffalo NY, US |
| Decision | Substantially Equivalent, Sep 11, 1987 |
| Received | Aug 24, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K873391
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.