510(k) K003533 ยท JOJ Indicator, Physical/Chemical Sterilization Process
CROSS-CHECKS LF, MODEL CI 119/S &CI 119/L
| Applicant | Steritec Products, Inc., Castle Rock CO, US |
| Decision | Substantially Equivalent, Feb 7, 2001 |
| Received | Nov 16, 2000 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K003533
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.