510(k) K052314 ยท HIB Speculum, Vaginal, Nonmetal
DYNAREX VAGINAL SPECULA 4900, MODELS 4911-SMALL, 4912-MEDIUM, 4913-LARGE
| Applicant | Dynarex Corp., Orangeburg NY, US |
| Decision | Substantially Equivalent, Nov 9, 2005 |
| Received | Aug 25, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K052314
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.