510(k) K073297

GE LOGIQ P6 by General Electric Co. — Product Code IYN

K073297 is an FDA 510(k) premarket notification submitted by General Electric Co. for the device "GE LOGIQ P6". The FDA issued a decision of Substantially Equivalent on December 18, 2007. The device falls under product code IYN (System, Imaging, Pulsed Doppler, Ultrasonic), a Class II device regulated under 21 CFR 892.1550. General Electric Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 18, 2007
Date Received
November 23, 2007
Clearance Type
Special
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