WOUND PROTECTOR

FDA 510(k) Premarket Notification · Submission K120061 · Applicant: Covidien, Formerly US Surgical A Divison of Tyco H

Public Record 510(k) Submission Decision Date: 2012-03-27 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K120061.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K120061
Device Name
WOUND PROTECTOR
Product Code
GCJ
Decision Date
2012-03-27
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Gastroenterology, Urology (GU)
Clearance Type
Traditional
Third Party Flag
N
Date Received
2012-01-09

Related Establishments / Registrations

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