510(k) K791888 ยท EFQ Gauze/Sponge, Internal
CATHETER CARE KIT REORDER 7940&7941
| Applicant | Ascep, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 17, 1979 |
| Received | Sep 11, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K791888
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.