510(k) K960099 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
PENROSE DRAIN MODELS 6001 - 6007
| Applicant | Sil-Med Corp., Taunton MA, US |
| Decision | Substantially Equivalent, Mar 11, 1996 |
| Received | Jan 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960099
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.