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PITON(TM) Y-PACK AND PITON(TM) TRI-PACK)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K945461
510(k) Type
Traditional
Applicant
MEDTRONICS INTERVENTIONAL VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1995
Days to Decision
88 days
Submission Type
Summary

PITON(TM) Y-PACK AND PITON(TM) TRI-PACK)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K945461
510(k) Type
Traditional
Applicant
MEDTRONICS INTERVENTIONAL VASCULAR
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/3/1995
Days to Decision
88 days
Submission Type
Summary