Last synced on 9 May 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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