510(k) K014248 ยท KNA Instrument, Manual, Specialized Obstetric-Gynecologic
DND 202 MANUAL UROLOGICAL DIGITAL NEEDLE DRIVER
| Applicant | Urogyn , Ltd., Ramat-Gan, IL |
| Decision | Substantially Equivalent, Mar 21, 2002 |
| Received | Dec 26, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K014248
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.