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

SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR

K Number: K970999 · Decision May 20, 1997
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
6
Review Days
62

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Basic Information

Device Name
SONY PGM-100P1MD TRINITRON COLOR GRAPHIC MONITOR
K Number
K970999
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sony Medical Systems
Date Received
March 19, 1997
Decision Date
May 20, 1997
Product Code
JAK
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
JAK System, X-Ray, Tomography, Computed

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