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

TECHNICON RA(R) SYSTEMS & ASSIST(R) CLIN. ANALYZER

K Number: K871892 · Decision Jun 17, 1987
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
117
Applicant Total
157
Review Days
33

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Basic Information

Device Name
TECHNICON RA(R) SYSTEMS & ASSIST(R) CLIN. ANALYZER
K Number
K871892
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1775
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Technicon Instruments Corp.
Date Received
May 15, 1987
Decision Date
June 17, 1987
Product Code
KNK
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
KNK Acid, Uric, Uricase (Colorimetric)

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