510(k) K871856
K871856 is an FDA 510(k) premarket notification submitted by Advanced Technology Laboratories, Inc. for the device "ANNULAR ARRAY SCANHEAD". The FDA issued a decision of SN on August 28, 1987. The device falls under product code HGL (Transducer, Ultrasonic, Obstetric), a Class II device regulated under 21 CFR 884.2960. Advanced Technology Laboratories, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- August 28, 1987
- Date Received
- May 12, 1987
- 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