510(k) K992071

TRANSVAGINAL ULTRASOUND PROBE HOLDER DEVICE by Ron-Tech Medical , Ltd. — Product Code HDC

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 27, 1999
Date Received
June 18, 1999
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tenaculum, Uterine
Device Class
Class II
Regulation Number
884.4530
Review Panel
OB
Submission Type