FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DIRECT BILIRUBIN

K Number: K930679 · Decision Jun 29, 1993
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
234
Applicant Total
7
Review Days
140

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Basic Information

Device Name
DIRECT BILIRUBIN
K Number
K930679
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1110
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Horizon Diagnostics, Inc.
Date Received
February 9, 1993
Decision Date
June 29, 1993
Product Code
CIG
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
CIG Diazo Colorimetry, Bilirubin

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Other Clearances by Horizon Diagnostics, Inc.

K Number Device Name
K971566 CREATINE KINASE-MB REAGENT SET
K933722 HORIZON DIAGNOSTICS TRIGLYCERIDES-GPO REAGENT
K935712 IRON/TIBC REAGENT
K930678 AMYLASE
K934533 BUN-300/BUN-500 UREA NITROGEN REAGENT
K930074 IN-VITRO DIAGNOSTIC REAGENT SET