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

VITROS IMMUNODIAGNOSTIC PRODUCTS NT PRO-BNP REAGENT PACK,CALIBRATORS,RANGE VERIFIERS,680 2156,680 2157,680 2158

K Number: K060632 · Decision Jun 6, 2006
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
44
Applicant Total
106
Review Days
89

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Basic Information

Device Name
VITROS IMMUNODIAGNOSTIC PRODUCTS NT PRO-BNP REAGENT PACK,CALIBRATORS,RANGE VERIFIERS,680 2156,680 2157,680 2158
K Number
K060632
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1117
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ortho-Clinical Diagnostics, Inc.
Date Received
March 9, 2006
Decision Date
June 6, 2006
Product Code
NBC
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
NBC Test, Natriuretic Peptide

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