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

MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC

K Number: K896309 · Decision Jan 12, 1990
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
24
Review Days
72

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Basic Information

Device Name
MAGNAVIEW M.R.I. VERSIONS 110FH & 110FM W/CARDIAC
K Number
K896309
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Instrumentarium Imaging, Inc.
Date Received
November 1, 1989
Decision Date
January 12, 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

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K955411 DELTA 16
K925987 INSTRUMENTARIUM MEGA4 HT
K924921 INSTRUMENTARIUM MEGA4 HT
K923581 INSTRUMENTARIUM MEGA4 HT
K924472 INSTRUMENTARIUM MEGA4 HT
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