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

KODAK EKTACHEM DT SLIDES (PHOS)

K Number: K874577 · Decision Jan 21, 1988
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
104
Applicant Total
238
Review Days
76

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Basic Information

Device Name
KODAK EKTACHEM DT SLIDES (PHOS)
K Number
K874577
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1580
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Eastman Kodak Company
Date Received
November 6, 1987
Decision Date
January 21, 1988
Product Code
CEO
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
CEO Phosphomolybdate (Colorimetric), Inorganic Phosphorus

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Other Clearances by Eastman Kodak Company

K Number Device Name
K060550 KODAK DIRECTVIEW DR 3000 SYSTEM 64KW/80KW GENERATORS, MODELS 6551345, 6551386
K060137 KODAK ECLIPSE IMAGE PROCESSING SOFTWARE
K060079 KODAK MODEL CR-7400 DIGITAL RADIOGRAPHY SYSTEM
K060055 KODAK PACS
K053347 KODAK CARESTREAM PACS
K051483 KODAK DIRECTVIEW DR SYSTEM DETECTOR
K051258 KODAK DIRECTVIEW DR 7500 SYSTEM, MODEL 8791345
K042159 KODAK COLOR MEDICAL IMAGER 1000
K042158 KODAK MEDICAL IMAGER 300
K040378 KODAK DIRECTVIEW CR CASSETTE/GP/15 X 30 CM, CATALOG# 8418253
Search all 238 clearances from Eastman Kodak Company →