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

MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC.

K Number: K800523 · Decision Mar 20, 1980
Classifications
1
FEI Numbers
85
Registration Numbers
85
Same Product Code
257
Applicant Total
86
Review Days
14

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Basic Information

Device Name
MONEL 80&90 ULTRAVIOLET-VISIBLE SPEC.
K Number
K800523
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2300
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Varian Assoc., Inc.
Date Received
March 6, 1980
Decision Date
March 20, 1980
Product Code
JJQ
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
JJQ Colorimeter, Photometer, Spectrophotometer For Clinical Use

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