510(k) K071754 ยท HDX Dilator, Vaginal
NEO-VAGINA SURGERY SET AND ACCESSORIES
| Applicant | KARL STORZ Endoscopy-America, Inc., Culver City CA, US |
| Decision | Substantially Equivalent, Jan 7, 2009 |
| Received | Jun 28, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071754
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.