TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE— 510(k) K992071
Substantially EquivalentRon-Tech Medical , Ltd.
FDA 510(k) clearance K992071 for TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE, Substantially Equivalent on 1999-08-27. Applicant: Ron-Tech Medical , Ltd..
Clearance details
- Applicant
- Ron-Tech Medical , Ltd.
- Product code
- Code HDC
- Advisory panel
- Obstetrics/Gynecology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Ginot, Shomron, IL
Data sourced from openFDA. This site is unofficial and independent of the FDA.