510(k) K923355 ยท KCF Dilator, Esophageal, Ent
PHARYNGEAL SALIVARY BYPASS TUBE
| Applicant | Boston Medical Products, Inc., Waltham MA, US |
| Decision | Substantially Equivalent, Oct 6, 1992 |
| Received | Jul 8, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923355
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.