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CLINITEK ATLAS PRO 12 REAGENT PAK SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K021428
510(k) Type
Traditional
Applicant
Bayer Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2002
Days to Decision
63 days
Submission Type
Summary

CLINITEK ATLAS PRO 12 REAGENT PAK SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K021428
510(k) Type
Traditional
Applicant
Bayer Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2002
Days to Decision
63 days
Submission Type
Summary