FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

GAMMA CAMERAS -GXA-301 & GCA-402

K Number: K771599 · Decision Sep 20, 1977
Classifications
1
FEI Numbers
26
Registration Numbers
26
Same Product Code
129
Applicant Total
54
Review Days
32

Basic Information

Device Name
GAMMA CAMERAS -GXA-301 & GCA-402
K Number
K771599
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1100
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
TOSHIBA MEDICAL SYSTEMS
Date Received
August 19, 1977
Decision Date
September 20, 1977
Product Code
IYX
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
IYX Camera, Scintillation (Gamma)

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