510(k) K810530 ยท KGZ Accessories, Catheter
PERI-PATCH GLUE MOLD
| Applicant | Quinton, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 24, 1981 |
| Received | Feb 26, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810530
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.