510(k) K023004 ยท EOB Nasopharyngoscope (Flexible Or Rigid)
LFRE INDIRECT LARYNGOSCOPE
| Applicant | Astralite Corp., Van Nuys CA, US |
| Decision | Substantially Equivalent, Jan 28, 2003 |
| Received | Sep 9, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K023004
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.