510(k) K143532 ยท NUC Lubricant, Personal
Durex Silicone
| Applicant | Reckitt Benckiser, LLC, Parsippany NJ, US |
| Decision | Substantially Equivalent, Jul 31, 2015 |
| Received | Dec 12, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K143532
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.