510(k) K952031

ULTRASOUND TRANSDUCER, MODEL US917 by Advanced Medical Systems, Inc. — Product Code HGL

K952031 is an FDA 510(k) premarket notification submitted by Advanced Medical Systems, Inc. for the device "ULTRASOUND TRANSDUCER, MODEL US917". The FDA issued a decision of Substantially Equivalent on July 18, 1995. The device falls under product code HGL (Transducer, Ultrasonic, Obstetric), a Class II device regulated under 21 CFR 884.2960. Advanced Medical Systems, Inc. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 18, 1995
Date Received
May 1, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Transducer, Ultrasonic, Obstetric
Device Class
Class II
Regulation Number
884.2960
Review Panel
OB
Submission Type