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INTRODUCER SHEATH, VESSEL DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992309
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
10/7/1999
Days to Decision
90 days
Submission Type
Summary

INTRODUCER SHEATH, VESSEL DILATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K992309
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent - Kit
Decision Date
10/7/1999
Days to Decision
90 days
Submission Type
Summary