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ACCUSTRIP HCG-URINE MODEL NUMBER HCG-002

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981838
510(k) Type
Traditional
Applicant
UNOTECH DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/1998
Days to Decision
30 days
Submission Type
Summary

ACCUSTRIP HCG-URINE MODEL NUMBER HCG-002

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981838
510(k) Type
Traditional
Applicant
UNOTECH DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/25/1998
Days to Decision
30 days
Submission Type
Summary