510(k) K952031
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