510(k) K041563 ยท LFD Saliva, Artificial
OASIS DRY MOUTH RELIEF DISCS OR OASIS MOUTH MOISTURIZING DISCS
| Applicant | Glaxosmithkline Consumer Healthcare, L.P., Parsippany NJ, US |
| Decision | Substantially Equivalent, Aug 27, 2004 |
| Received | Jun 10, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041563
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.