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OCCLUSION BALLOON CATHETER, MODEL VENOS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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