510(k) K822032 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
LARGE VOLUME CLOSED WOUND SUCTION DRAIN
| Applicant | American Heyer Schulte, Walker MI, US |
| Decision | Substantially Equivalent, Aug 16, 1982 |
| Received | Jul 12, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K822032
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.