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ACCUTEST HCG-URINE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971886
510(k) Type
Traditional
Applicant
Unotech Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1997
Days to Decision
20 days
Submission Type
Summary

ACCUTEST HCG-URINE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971886
510(k) Type
Traditional
Applicant
Unotech Diagnostics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/11/1997
Days to Decision
20 days
Submission Type
Summary