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INTRODUCER, PERCUTANEOUS SELDINGER

Page Type
Cleared 510(K)
510(k) Number
K812964
510(k) Type
Traditional
Applicant
TRIAD MEDICAL DIVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1981
Days to Decision
25 days

INTRODUCER, PERCUTANEOUS SELDINGER

Page Type
Cleared 510(K)
510(k) Number
K812964
510(k) Type
Traditional
Applicant
TRIAD MEDICAL DIVISION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1981
Days to Decision
25 days