1.5 GE 6-CHANNEL Phased Array Flex Coil, 3.0 GE 6-CHANNEL Phased Array Flex Coil

FDA 510(k) K110610 · Ge Medical Systems, LLC

Substantially Equivalent

510(k) numberK110610

Submission

Device name
1.5 GE 6-CHANNEL Phased Array Flex Coil, 3.0 GE 6-CHANNEL Phased Array Flex Coil
Applicant
Ge Medical Systems, LLC
Waukesha, WI, US
Received
March 3, 2011
Decision date
April 1, 2011
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MOS – Coil, Magnetic Resonance, Specialty
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1000
Specialty
Radiology

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Questions and answers

When was 1.5 GE 6-CHANNEL Phased Array Flex Coil, 3.0 GE 6-CHANNEL Phased Array Flex Coil cleared by the FDA?

1.5 GE 6-CHANNEL Phased Array Flex Coil, 3.0 GE 6-CHANNEL Phased Array Flex Coil (K110610) received a 510(k) decision of Substantially Equivalent on April 1, 2011, 29 days after the submission was received.

What is the product code of K110610?

The FDA product code is MOS – Coil, Magnetic Resonance, Specialty, a Class II (moderate risk) device regulated under 21 CFR 892.1000.