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MINISTRIP/ SERUM AND URINE COMBO HCG TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974060
510(k) Type
Traditional
Applicant
INTERNATIONAL NEWTECH DEVELOPMENT, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/9/1998
Days to Decision
164 days
Submission Type
Statement

MINISTRIP/ SERUM AND URINE COMBO HCG TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974060
510(k) Type
Traditional
Applicant
INTERNATIONAL NEWTECH DEVELOPMENT, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
4/9/1998
Days to Decision
164 days
Submission Type
Statement