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

GRIFFIN SPECT/CT IMAGING SYSTEM

K Number: K041218 · Decision May 24, 2004
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
470
Applicant Total
88
Review Days
14

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Basic Information

Device Name
GRIFFIN SPECT/CT IMAGING SYSTEM
K Number
K041218
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1200
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Adac Laboratories
Date Received
May 10, 2004
Decision Date
May 24, 2004
Product Code
KPS
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

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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K042903 AUTOSPECS
K041577 PINNACLE3 RADIATION THERAPY PLANNING SYSTEM
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K040326 AUTOQUANT PLUS
K040142 ENSPHERE TEMPO JETSTREAM WORKSPACE CARDIOLOGY MODULE
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