Last synced on 14 November 2025 at 11:06 pm

GUIDING CATHETER HEMOSTASIS VALVE CAP

Page Type
Cleared 510(K)
510(k) Number
K933033
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1993
Days to Decision
80 days
Submission Type
Statement

GUIDING CATHETER HEMOSTASIS VALVE CAP

Page Type
Cleared 510(K)
510(k) Number
K933033
510(k) Type
Traditional
Applicant
ARROW INTL., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/10/1993
Days to Decision
80 days
Submission Type
Statement