510(k) K951113 ยท LRT Indicator, Sterilization
CROSS-CHECKS
| Applicant | Steritec Products Mfg Co, Inc., Castle Rock CO, US |
| Decision | Substantially Equivalent, Aug 19, 1996 |
| Received | Mar 10, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951113
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.