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MODIFICATION TO VASCULAR CLOSURE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K012362
510(k) Type
Special
Applicant
STD MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2001
Days to Decision
29 days
Submission Type
Summary

MODIFICATION TO VASCULAR CLOSURE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K012362
510(k) Type
Special
Applicant
STD MFG., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2001
Days to Decision
29 days
Submission Type
Summary