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

FLEXART QD HEAD/NECK COIL

K Number: K961391 · Decision Jul 9, 1996
Classifications
1
FEI Numbers
75
Registration Numbers
75
Same Product Code
487
Applicant Total
68
Review Days
90

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Basic Information

Device Name
FLEXART QD HEAD/NECK COIL
K Number
K961391
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Toshiba America Mri, Inc.
Date Received
April 10, 1996
Decision Date
July 9, 1996
Product Code
MOS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MOS), ordered by most recent decision date.

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Other Clearances by Toshiba America Mri, Inc.

K Number Device Name
K002531 EXCELART WITH PIANISSIMO, MODEL MRT-1501/P3
K002522 OPART, MODEL MRT-600
K000549 OPART, MODEL MRT-600
K993803 EXCELART WITH PIANISSIMO
K993574 OPART/PRODIGA, OPART/PROTENZA, OPART/PARAGON
K991740 OPART, MODEL MRT-600
K991057 EXTRA LARGE BODY COIL FOR OPART (MRT-600)
K990620 EXCELART
K990260 OPART
K990007 OPART, MODEL MRT-600
Search all 68 clearances from Toshiba America Mri, Inc. →