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

SODIUM NITRITE

K Number: K760409 · Decision Nov 2, 1976
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
234
Applicant Total
54
Review Days
85

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Basic Information

Device Name
SODIUM NITRITE
K Number
K760409
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1110
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
J.T. Baker Chemical Co.
Date Received
August 9, 1976
Decision Date
November 2, 1976
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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K801909 LSA 290 ASSAY REAGENTS/NEPHELOMETRIC
K801662 J.T. BAKER ALPHA-2-MACROGLOBULIN NEPH.
K801669 J.T. BAKER ALPHA-1-ANTITRYPSIN NEPHELO
K801661 J.T. BAKER CERULOPLASMIN NEPHELOMETRIC
K801795 BAKER DIAGNOSTIC ULTRA-RATE SODIUM/POT.
K801362 ALBUMIN NEPHELOMETRIC ASSAY
K801432 HEMOPEXIN NEPHELOMETRIC ASSAY
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