510(k) K063159 ยท MED Sterilant, Medical Devices
STERILOX LIQUID CHEMICAL STERILANT SYSTEM
| Applicant | Puricore, Inc., Radnor PA, US |
| Decision | Substantially Equivalent, Apr 2, 2007 |
| Received | Oct 17, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063159
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.