510(k) K802214 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
COS-UPHOFF INT'L DS-5 DRAINAGE SYSTEM
| Applicant | Cox-Uphuff Intl., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 23, 1980 |
| Received | Sep 12, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802214
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.