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

KODAK EKTASCAN IMAGE TRANSMISSION SYSTEM P1

K Number: K864739 · Decision Feb 11, 1987
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
238
Review Days
69

Basic Information

Device Name
KODAK EKTASCAN IMAGE TRANSMISSION SYSTEM P1
K Number
K864739
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
EASTMAN KODAK COMPANY
Date Received
December 4, 1986
Decision Date
February 11, 1987
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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