510(k) K151910

Ultrasound Scanner System BK2300 by Bk Medical Aps — Product Code IYN

K151910 is an FDA 510(k) premarket notification submitted by Bk Medical Aps for the device "Ultrasound Scanner System BK2300". The FDA issued a decision of Substantially Equivalent on October 5, 2015. The device falls under product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic), a Class II device regulated under 21 CFR 892.1550. Bk Medical Aps has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 5, 2015
Date Received
July 13, 2015
Clearance Type
Abbreviated
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