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

MAGNETIC RESONANCE DIAGNOSTIC DEVICE

K Number: K903319 · Decision Aug 17, 1990
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
169
Review Days
23

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Basic Information

Device Name
MAGNETIC RESONANCE DIAGNOSTIC DEVICE
K Number
K903319
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
GE Medical Systems
Date Received
July 25, 1990
Decision Date
August 17, 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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