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

KODAK MIN-R 2 CASSETTE

K Number: K890361 · Decision Feb 24, 1989
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
50
Applicant Total
238
Review Days
30

Basic Information

Device Name
KODAK MIN-R 2 CASSETTE
K Number
K890361
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1850
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
EASTMAN KODAK COMPANY
Date Received
January 25, 1989
Decision Date
February 24, 1989
Product Code
IXA
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
IXA Cassette, Radiographic Film

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