510(k) K911756 ยท ECB Unit, Syringe, Air And/Or Water
POSTERIOR NASAL EPISTAXIS INSTRUMENTS
| Applicant | Richard Wolf Medical Instruments Corp., Rosemont IL, US |
| Decision | Substantially Equivalent, Oct 24, 1991 |
| Received | Apr 18, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911756
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.