Last synced on 25 January 2026 at 3:41 am

UNIMARK HOME PREGNANCY TEST DEVICE

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