510(k) K992071 ยท HDC Tenaculum, Uterine
TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE
| Applicant | Ron-Tech Medical , Ltd., Ginot, Shomron, IL |
| Decision | Substantially Equivalent, Aug 27, 1999 |
| Received | Jun 18, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992071
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.