Pacific Plus PTA Catheter

FDA 510(k) Premarket Notification · Submission K202800 · Applicant: Medtronic Vascular,Inc(Formerly D.B.A Ev3 Inc.,Covidien, LLC)

Public Record 510(k) Submission Decision Date: 2020-11-18 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K202800.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K202800
Device Name
Pacific Plus PTA Catheter
Product Code
LIT
Decision Date
2020-11-18
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Cardiovascular (CV)
Clearance Type
Traditional
Third Party Flag
N
Date Received
2020-09-23

Related Establishments / Registrations

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