510(k) K860568
K860568 is an FDA 510(k) premarket notification submitted by Interspec, Inc. for the device "ULTRASONIC IMAGING SYSTEM (MODIFIED)". The FDA issued a decision of SN on August 11, 1986. The device falls under product code ITX (Transducer, Ultrasonic, Diagnostic), a Class II device regulated under 21 CFR 892.1570. Interspec, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- August 11, 1986
- Date Received
- February 14, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Transducer, Ultrasonic, Diagnostic
- Device Class
- Class II
- Regulation Number
- 892.1570
- Review Panel
- RA
- Submission Type