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DYMAX ENDOVAGINAL BIOPSY GUIDE

Page Type
Cleared 510(K)
510(k) Number
K894415
510(k) Type
Traditional
Applicant
DYMAX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1989
Days to Decision
100 days

DYMAX ENDOVAGINAL BIOPSY GUIDE

Page Type
Cleared 510(K)
510(k) Number
K894415
510(k) Type
Traditional
Applicant
DYMAX CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/1989
Days to Decision
100 days