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INTRODUCER, PERCUTANEOUS

Page Type
Cleared 510(K)
510(k) Number
K812143
510(k) Type
Traditional
Applicant
WILLSON
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1981
Days to Decision
21 days

INTRODUCER, PERCUTANEOUS

Page Type
Cleared 510(K)
510(k) Number
K812143
510(k) Type
Traditional
Applicant
WILLSON
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/18/1981
Days to Decision
21 days