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KERATIN PRIMARY ANTIBODY

Page Type
Cleared 510(K)
510(k) Number
K935161
510(k) Type
Traditional
Applicant
VENTANA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1996
Days to Decision
875 days
Submission Type
Summary

KERATIN PRIMARY ANTIBODY

Page Type
Cleared 510(K)
510(k) Number
K935161
510(k) Type
Traditional
Applicant
VENTANA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/1996
Days to Decision
875 days
Submission Type
Summary