510(k) K960513 ยท MED Sterilant, Medical Devices
PERACT 20 LIQUID STERILANT
| Applicant | Minntech Corp., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 1, 1997 |
| Received | Feb 5, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960513
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.