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OCCLUSION BALLOON CATHETER, MODEL VENOS

Page Type
Cleared 510(K)
510(k) Number
K081052
510(k) Type
Traditional
Applicant
Oscor Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2008
Days to Decision
65 days
Submission Type
Statement

OCCLUSION BALLOON CATHETER, MODEL VENOS

Page Type
Cleared 510(K)
510(k) Number
K081052
510(k) Type
Traditional
Applicant
Oscor Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/18/2008
Days to Decision
65 days
Submission Type
Statement