510(k) K790654 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
CLOSED WOUND VACUUM DRAINAGE SYSTEM
| Applicant | 3M Company, White City OR, US |
| Decision | Substantially Equivalent, Apr 26, 1979 |
| Received | Apr 5, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790654
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.