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

OLYMPUS AU 5000 FLAME PHOTOMETER MODULE

K Number: K862148 · Decision Sep 29, 1986
Classifications
1
FEI Numbers
1
Registration Numbers
1
Same Product Code
21
Applicant Total
142
Review Days
117

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Basic Information

Device Name
OLYMPUS AU 5000 FLAME PHOTOMETER MODULE
K Number
K862148
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2540
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Olympus Corp.
Date Received
June 4, 1986
Decision Date
September 29, 1986
Product Code
JJO
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
JJO Flame Emission Photometer For Clinical Use

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