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

GATED MIBI 3-D EJECTION FRACTION PROCESSING

K Number: K961597 · Decision Sep 4, 1996
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
459
Applicant Total
16
Review Days
133

Basic Information

Device Name
GATED MIBI 3-D EJECTION FRACTION PROCESSING
K Number
K961597
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1200
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
TRIONIX RESEARCH LABORATORY, INC.
Date Received
April 24, 1996
Decision Date
September 4, 1996
Product Code
KPS
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
KPS System, Tomography, Computed, Emission

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