Last synced on 25 January 2026 at 3:41 am

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

Page Type
Cleared 510(K)
PDF
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
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