510(k) K091419 ยท LFD Saliva, Artificial
VICKS POWERSHOT DRY THROAT & MOUTH RELIEF
| Applicant | The Procter & Gamble Co., Mason OH, US |
| Decision | Substantially Equivalent, Aug 28, 2009 |
| Received | May 13, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091419
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.