510(k) K101477 ยท LFD Saliva, Artificial
BIOTENE DRY MOUTH MOUTHWASH, BIOTENE PBF DRY MOUTH MOUTHWASH
| Applicant | Glaxosmithkline Consumer Healthcare (Gskch), Parsippany NJ, US |
| Decision | Substantially Equivalent, Sep 28, 2010 |
| Received | May 28, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101477
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.