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

DIGITAL IMAGE PROCESSOR FP-2C

K Number: K850080 · Decision Apr 19, 1985
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
4
Review Days
99

Basic Information

Device Name
DIGITAL IMAGE PROCESSOR FP-2C
K Number
K850080
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
EIGEN VIDEO
Date Received
January 10, 1985
Decision Date
April 19, 1985
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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