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GENERAL SEMEN ANALYSIS KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071737
510(k) Type
Traditional
Applicant
Dyn-Bioshaf (2006) , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2007
Days to Decision
121 days
Submission Type
Statement

GENERAL SEMEN ANALYSIS KIT

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071737
510(k) Type
Traditional
Applicant
Dyn-Bioshaf (2006) , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2007
Days to Decision
121 days
Submission Type
Statement