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

VACUETTE TRACE ELEMENTS TUBES

K Number: K023971 · Decision Jan 27, 2003
Classifications
1
FEI Numbers
222
Registration Numbers
222
Same Product Code
230
Applicant Total
5
Review Days
59

Basic Information

Device Name
VACUETTE TRACE ELEMENTS TUBES
K Number
K023971
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1675
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
GREINER BIO-ONE VACUETTE NORTH AMERICA
Date Received
November 29, 2002
Decision Date
January 27, 2003
Product Code
JKA
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
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection

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