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A1CNOW+ (10 TEST KIT, PROFESSIONAL USE) MODEL 3024, A1CNOW+(20 TEST KIT, PROFESSIONAL USE) MODEL 3021, A1CNOW SELF CHEC

Page Type
Cleared 510(K)
510(k) Number
K090413
510(k) Type
Special
Applicant
BAYER HEALTHCARE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2009
Days to Decision
85 days
Submission Type
Summary

A1CNOW+ (10 TEST KIT, PROFESSIONAL USE) MODEL 3024, A1CNOW+(20 TEST KIT, PROFESSIONAL USE) MODEL 3021, A1CNOW SELF CHEC

Page Type
Cleared 510(K)
510(k) Number
K090413
510(k) Type
Special
Applicant
BAYER HEALTHCARE, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/14/2009
Days to Decision
85 days
Submission Type
Summary