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SPERMCHECK VASECTOMY

Page Type
Cleared 510(K)
510(k) Number
K073039
510(k) Type
Traditional
Applicant
PRINCETON BIOMEDITECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/2008
Days to Decision
87 days
Submission Type
Summary

SPERMCHECK VASECTOMY

Page Type
Cleared 510(K)
510(k) Number
K073039
510(k) Type
Traditional
Applicant
PRINCETON BIOMEDITECH CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/2008
Days to Decision
87 days
Submission Type
Summary