510(k) K131209
K131209 is an FDA 510(k) premarket notification submitted by Teratech Corp. for the device "TERASON USMART3200T ULTRASOUND SYSTEM". The FDA issued a decision of Substantially Equivalent on May 24, 2013. 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
- May 24, 2013
- Date Received
- Apr 29, 2013
- 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)