510(k) K110482
K110482 is an FDA 510(k) premarket notification submitted by Teratech Corp. for the device "PROSOUND C3 / C3 CV ULTRASOUND SYSTEMS". The FDA issued a decision of Substantially Equivalent on Mar 18, 2011. The device falls under product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic), a Class II device regulated under 21 CFR 892.1550. Teratech Corp. has 16 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Mar 18, 2011
- Date Received
- Feb 18, 2011
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, Imaging, Pulsed Doppler, Ultrasonic
- Device Class
- Class II
- Regulation Number
- 892.1550
- Review Panel
- RA
- Submission Type
- 510(k)