VERSAPORT V2 BLADELESS OPTIICAL TROCAR AND/OR VERSAPORT BLADELESS OPTICAL TROCAR

FDA 510(k) Premarket Notification · Submission K112349 · Applicant: Covidien, Formerly US Surgical A Divison of Tyco H

Public Record 510(k) Submission Decision Date: 2011-09-01 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K112349.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K112349
Device Name
VERSAPORT V2 BLADELESS OPTIICAL TROCAR AND/OR VERSAPORT BLADELESS OPTICAL TROCAR
Product Code
GCJ
Decision Date
2011-09-01
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Gastroenterology, Urology (GU)
Clearance Type
Special
Third Party Flag
N
Date Received
2011-08-16

Related Establishments / Registrations

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