FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

3.0T TORSO PHASED ARRAY COIL

K Number: K030495 · Decision Mar 5, 2003
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
487
Applicant Total
54
Review Days
14

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Basic Information

Device Name
3.0T TORSO PHASED ARRAY COIL
K Number
K030495
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ge Medical Systems, Inc.
Date Received
February 19, 2003
Decision Date
March 5, 2003
Product Code
MOS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MOS Coil, Magnetic Resonance, Specialty

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Other Clearances by Ge Medical Systems, Inc.

K Number Device Name
K091673 GE LIGHTSPEED ACT FP16
K082104 GE LIGHTSPEED RT16 / LIGHTSPEED XTRA V2 CT SYSTEM (AKA GE LIGHTSPEED RT16 / LIGHTSPEED XTRA CT SYSTEM
K042844 GE SIGNA EXCITE 1.5T 6 CHANNEL PHASED ARRAY FLEX COIL, GE SIGNA EXCITE 3.0T 6 CHANNEL PHASED ARRAY FLEX COIL
K042053 INNOVA 4100, INNOVA 3100
K040125 SENOGRAPHIC STEREO
K033244 DIGITAL FLUOROSCOPIC IMAGING SYSTEM, MODEL INNOVA 4100 WITH TILT TABLE OPTION
K031209 GE 1.5T 8 CHANNEL TORSO COIL
K023943 CT COLONOGRAPHY
K030934 GE LOGIQ 9 MODEL 2375600
K030953 GE 3.0T GENERAL PURPOSE FLEX COIL
Search all 54 clearances from Ge Medical Systems, Inc. →