510(k) K041321 ยท HET Laparoscope, Gynecologic (And Accessories)
VEROSCOPE OPTICAL VERESS CANNULA & DILATION TUBE SYSTEM
| Applicant | Richard Wolf Medical Instruments Corp., Vernon Hills IL, US |
| Decision | Substantially Equivalent, Jul 9, 2004 |
| Received | May 18, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041321
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.