510(k) K170303

E5 Series Digital Color Doppler Ultrasound System by Sonoscape Medical Corp. — Product Code IYN

K170303 is an FDA 510(k) premarket notification submitted by Sonoscape Medical Corp. for the device "E5 Series Digital Color Doppler Ultrasound System". The FDA issued a decision of Substantially Equivalent on May 19, 2017. The device falls under product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic), a Class II device regulated under 21 CFR 892.1550. Sonoscape Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 19, 2017
Date Received
January 31, 2017
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Imaging, Pulsed Doppler, Ultrasonic
Device Class
Class II
Regulation Number
892.1550
Review Panel
RA
Submission Type