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ACON HCG ONE STEP PREGNANCY TEST DEVICE (URINE)

Page Type
Cleared 510(K)
510(k) Number
K993317
510(k) Type
Traditional
Applicant
ACON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1999
Days to Decision
58 days
Submission Type
Summary

ACON HCG ONE STEP PREGNANCY TEST DEVICE (URINE)

Page Type
Cleared 510(K)
510(k) Number
K993317
510(k) Type
Traditional
Applicant
ACON LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/1999
Days to Decision
58 days
Submission Type
Summary