510(k) K032585 ยท HDC Tenaculum, Uterine
TRANSVAGINAL ULTRASOUND PROBE HOLDER SYSTEM
| Applicant | Ron-Tech Medical , Ltd., Petach-Tikva, IL |
| Decision | Substantially Equivalent, Jan 9, 2004 |
| Received | Aug 21, 2003 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K032585
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.