510(k) K960441 ยท JOJ Indicator, Physical/Chemical Sterilization Process
STERITEC INTEGRAPH MODEL CI-101
| Applicant | Steritec Products Mfg Co, Inc., Aurora CO, US |
| Decision | Substantially Equivalent, May 8, 1997 |
| Received | Feb 1, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960441
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.