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

MRT35-SP

K Number: K905442 · Decision Dec 21, 1990
Classifications
1
FEI Numbers
152
Registration Numbers
152
Same Product Code
1071
Applicant Total
68
Review Days
87

Basic Information

Device Name
MRT35-SP
K Number
K905442
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
TOSHIBA AMERICA MRI, INC.
Date Received
September 25, 1990
Decision Date
December 21, 1990
Product Code
LNH
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
LNH System, Nuclear Magnetic Resonance Imaging

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LNH), 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. →