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

BILIRUBIN PROCEDURE, TEKPOINT TOT & DIR.

K Number: K770458 · Decision May 10, 1977
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
234
Applicant Total
30
Review Days
63

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Basic Information

Device Name
BILIRUBIN PROCEDURE, TEKPOINT TOT & DIR.
K Number
K770458
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1110
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Icn Pharmaceuticals, Inc.
Date Received
March 8, 1977
Decision Date
May 10, 1977
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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