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

PROCEDURE NO. 552/553 BILIRUBIN, TOTAL AND DIRECT

K Number: K872197 · Decision Aug 13, 1987
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
233
Applicant Total
164
Review Days
66

Basic Information

Device Name
PROCEDURE NO. 552/553 BILIRUBIN, TOTAL AND DIRECT
K Number
K872197
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1110
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
SIGMA DIAGNOSTICS, INC.
Date Received
June 8, 1987
Decision Date
August 13, 1987
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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