FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

BD VIPER INSTRUMENT

K Number: K023955 · Decision Jun 24, 2003
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
139
Applicant Total
190
Review Days
209

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Basic Information

Device Name
BD VIPER INSTRUMENT
K Number
K023955
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2750
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Becton, Dickinson & CO
Date Received
November 27, 2002
Decision Date
June 24, 2003
Product Code
JQW
Advisory Committee
Clinical Chemistry
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JQW Station, Pipetting And Diluting, For Clinical Use

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