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

DISPLAY PROCESSOR - MODEL IDP5100

K Number: K920550 · Decision Apr 13, 1992
Classifications
1
FEI Numbers
136
Registration Numbers
136
Same Product Code
299
Applicant Total
14
Review Days
67

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Basic Information

Device Name
DISPLAY PROCESSOR - MODEL IDP5100
K Number
K920550
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1650
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Perkins Mfg. Co.
Date Received
February 6, 1992
Decision Date
April 13, 1992
Product Code
JAA
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
JAA System, X-Ray, Fluoroscopic, Image-Intensified

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K915232 GRUNDIG ELECTRONICS VARIOUS MODELS
K910384 VIDEO ANNOTATOR MODEL PK2310
K904986 PROGRAMMABLE VIDEO CONTROLLER MODEL PK2060
K904540 VIDEO SYSTEM INTERFACE MODELS
K896615 CINE CAMERA CONTROL MODEL PK2037
K895500 PATIENT POSITIONING ACCESSORIES
K893644 PK2025/PK2045 PROGRAMMABLE VIDEO CONTROLLER
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