510(k) K010534 ยท JOJ Indicator, Physical/Chemical Sterilization Process
CROSS-CHECKS DUAL, MODEL CI 125
| Applicant | Steritec Products, Inc., Castle Rock CO, US |
| Decision | Substantially Equivalent, Aug 6, 2001 |
| Received | Feb 23, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K010534
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.