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HYBRID PERIPHERAL DILATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K834220
510(k) Type
Traditional
Applicant
AMERICAN EDWARDS LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/1984
Days to Decision
53 days

HYBRID PERIPHERAL DILATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K834220
510(k) Type
Traditional
Applicant
AMERICAN EDWARDS LABORATORIES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/27/1984
Days to Decision
53 days