510(k) K781400 ยท GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered
HEMOVAC TUBING MATERIAL CHANGE
| Applicant | Snyder Laboratories, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 20, 1978 |
| Received | Aug 15, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781400
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.