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RETRIEVAL DEVICE

Page Type
Cleared 510(K)
510(k) Number
K914067
510(k) Type
Traditional
Applicant
TARGET THERAPEUTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/1991
Days to Decision
90 days
Submission Type
Statement

RETRIEVAL DEVICE

Page Type
Cleared 510(K)
510(k) Number
K914067
510(k) Type
Traditional
Applicant
TARGET THERAPEUTICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/1991
Days to Decision
90 days
Submission Type
Statement