510(k) K962688 ยท KCF Dilator, Esophageal, Ent
MONTGOMERY RADIOPAQUE SALIVARY BYPASS TUBE
| Applicant | Boston Medical Products, Inc., Westborough MA, US |
| Decision | Substantially Equivalent, Jul 25, 1996 |
| Received | Jul 11, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K962688
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.