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

OPUS MAGNUM ANALYZER

K Number: K926131 · Decision Jun 7, 1993
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
37
Applicant Total
35
Review Days
182

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Basic Information

Device Name
OPUS MAGNUM ANALYZER
K Number
K926131
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2560
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Pb Diagnostic Systems, Inc.
Date Received
December 7, 1992
Decision Date
June 7, 1993
Product Code
KHO
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
KHO Fluorometer, For Clinical Use

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K935229 OPUS DIGITOXIN
K934705 OPUS NAPA
K933675 OPUS TOTAL CK
K933066 OPUS ESTRADIOL
K932279 OPUS(R) TOTAL B-HCG TEST SYSTEM
K924957 OPUS(R) VANCOMYCIN
Search all 35 clearances from Pb Diagnostic Systems, Inc. →