FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

KODAK EKTACHEM DT SLIDES (MG)

K Number: K874576 · Decision Jan 21, 1988
Classifications
1
FEI Numbers
44
Registration Numbers
44
Same Product Code
89
Applicant Total
238
Review Days
76

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Basic Information

Device Name
KODAK EKTACHEM DT SLIDES (MG)
K Number
K874576
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1495
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Eastman Kodak Company
Date Received
November 6, 1987
Decision Date
January 21, 1988
Product Code
JGJ
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JGJ Photometric Method, Magnesium

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K053347 KODAK CARESTREAM PACS
K051483 KODAK DIRECTVIEW DR SYSTEM DETECTOR
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K042159 KODAK COLOR MEDICAL IMAGER 1000
K042158 KODAK MEDICAL IMAGER 300
K040378 KODAK DIRECTVIEW CR CASSETTE/GP/15 X 30 CM, CATALOG# 8418253
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