510(k) K883079
K883079 is an FDA 510(k) premarket notification submitted by Ausonics Pty , Ltd. for the device "WWDS-005 HUMAN RECTAL PROBE". The FDA issued a decision of Substantially Equivalent on December 14, 1988. The device falls under product code IYO (System, Imaging, Pulsed Echo, Ultrasonic), a Class II device regulated under 21 CFR 892.1560. Ausonics Pty , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 14, 1988
- Date Received
- July 21, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Imaging, Pulsed Echo, Ultrasonic
- Device Class
- Class II
- Regulation Number
- 892.1560
- Review Panel
- RA
- Submission Type