510(k) K963839 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
CORDIS SUCTION RESERVOIR - MODEL NUMBER: 910-500
| Applicant | Cordis Corp., Miami Lakes FL, US |
| Decision | Substantially Equivalent, Dec 12, 1996 |
| Received | Sep 24, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963839
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.