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INTRAVASCULAR GUIDE WIRE AND EXTENSION WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924009
510(k) Type
Traditional
Applicant
PILOT CARDIOVASCULAR SYSTEMS, INC., SUB. C.R. BARD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1992
Days to Decision
88 days
Submission Type
Summary

INTRAVASCULAR GUIDE WIRE AND EXTENSION WIRE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K924009
510(k) Type
Traditional
Applicant
PILOT CARDIOVASCULAR SYSTEMS, INC., SUB. C.R. BARD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/1992
Days to Decision
88 days
Submission Type
Summary