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UNIMARK HOME PREGNANCY TEST DEVICE

Page Type
Cleared 510(K)
510(k) Number
K032992
510(k) Type
Traditional
Applicant
BIOTECH ATLANTIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2003
Days to Decision
57 days
Submission Type
Summary

UNIMARK HOME PREGNANCY TEST DEVICE

Page Type
Cleared 510(K)
510(k) Number
K032992
510(k) Type
Traditional
Applicant
BIOTECH ATLANTIC, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2003
Days to Decision
57 days
Submission Type
Summary