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ACON QUIK-CHECK II HOME PREGNANCY TEST STRIP

Page Type
Cleared 510(K)
510(k) Number
K033041
510(k) Type
Traditional
Applicant
ACON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2003
Days to Decision
53 days
Submission Type
Summary

ACON QUIK-CHECK II HOME PREGNANCY TEST STRIP

Page Type
Cleared 510(K)
510(k) Number
K033041
510(k) Type
Traditional
Applicant
ACON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2003
Days to Decision
53 days
Submission Type
Summary