510(k) K093371
K093371 is an FDA 510(k) premarket notification submitted by Dgh Technology, Inc. for the device "MODEL DGH 6000 SCANMATE A". The FDA issued a decision of Substantially Equivalent on Apr 5, 2010. The device falls under product code IYO (System, Imaging, Pulsed Echo, Ultrasonic), a Class II device regulated under 21 CFR 892.1560. Dgh Technology, Inc. has 6 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 5, 2010
- Date Received
- Oct 29, 2009
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- System, Imaging, Pulsed Echo, Ultrasonic
- Device Class
- Class II
- Regulation Number
- 892.1560
- Review Panel
- RA
- Submission Type
- 510(k)