510(k) K800577 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
SNYDER HEMOVAC TM VENTED WOUND KIT
| Applicant | Snyder Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 16, 1980 |
| Received | Mar 14, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800577
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.