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

QUANTEM

K Number: K963162 · Decision Nov 12, 1996
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
459
Applicant Total
94
Review Days
90

Basic Information

Device Name
QUANTEM
K Number
K963162
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1200
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ELSCINT, INC.
Date Received
August 14, 1996
Decision Date
November 12, 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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K974614 GYREX 2T PRESTIGE 100-6321-0107, GYREX PRIVILEDGE 100-6326-0102, GYREX PRIMA 1TG 100-6250-0102
K972592 2T PRESTIGE(100-6321-0107)/PRIVILEGE(100-6326-0102)/GYREX V-EP(100-6327-0101)
K970680 GLORY
K965044 GYREX 2T PRESTIGE MODEL NO. 100-6321-0107 AND GYREX PRIVILEGE MODEL NO. 100-6326-0102
K970980 CARDIAC SCORING FOR CT SCANNERS
K970005 GYREX 2T-PRESTIGE
Search all 94 clearances from ELSCINT, INC. →