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ARTERIAL EMBOLIZATION DEVICE (KRD)

Page Type
Cleared 510(K)
510(k) Number
K940982
510(k) Type
Traditional
Applicant
COOK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1994
Days to Decision
227 days
Submission Type
Statement

ARTERIAL EMBOLIZATION DEVICE (KRD)

Page Type
Cleared 510(K)
510(k) Number
K940982
510(k) Type
Traditional
Applicant
COOK, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/1994
Days to Decision
227 days
Submission Type
Statement