510(k) K992505
K992505 is an FDA 510(k) premarket notification submitted by Teratech Corp. for the device "TERATECH, MODEL 2000 IMAGING IMAGING". The FDA issued a decision of Substantially Equivalent on Nov 10, 1999. The device falls under product code IYO (System, Imaging, Pulsed Echo, Ultrasonic), a Class II device regulated under 21 CFR 892.1560. Teratech Corp. has 16 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Nov 10, 1999
- Date Received
- Jul 27, 1999
- 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
- 510(k)