TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE— 510(k) K992071

Name: FDA 510(k) clearance K992071
Creator: U.S. Food and Drug Administration
Published: 1999-08-27

Substantially Equivalent

Ron-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.. Device class: 2.

Clearance details

Applicant: Ron-Tech Medical , Ltd.
Product code: Code HDC
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1999-06-18
Decision date: 1999-08-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ginot, Shomron, IL

Download summary PDF View on FDA.gov ↗

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