510(k) K141312 ยท FRC Indicator, Biological Sterilization Process
STERILUCENT PROCESS CHALLENGE DEVICE
| Applicant | Sterilucent, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 31, 2014 |
| Received | May 20, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141312
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.