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ALLELIX PREGNANCY DETECTION KIT 48 TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871308
510(k) Type
Traditional
Applicant
ALLELIX, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/11/1987
Days to Decision
71 days

ALLELIX PREGNANCY DETECTION KIT 48 TEST KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K871308
510(k) Type
Traditional
Applicant
ALLELIX, INC.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/11/1987
Days to Decision
71 days