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MODIFICATION TO G2 FILTER SYSTEM-FEMORAL DELIVERY KIT, MODEL RF-310F

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062887
510(k) Type
Special
Applicant
Bard Peripheral Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2006
Days to Decision
30 days
Submission Type
Summary

MODIFICATION TO G2 FILTER SYSTEM-FEMORAL DELIVERY KIT, MODEL RF-310F

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K062887
510(k) Type
Special
Applicant
Bard Peripheral Vascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/2006
Days to Decision
30 days
Submission Type
Summary