LigaSure Maryland Jaw Thoracic Sealer/Divider One-step Sealing, Nano-coated

FDA 510(k) Premarket Notification · Submission K181085 · Applicant: Covidien

Public Record 510(k) Submission Decision Date: 2018-06-21 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K181085.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K181085
Applicant / Sponsor
Device Name
LigaSure Maryland Jaw Thoracic Sealer/Divider One-step Sealing, Nano-coated
Product Code
GEI
Decision Date
2018-06-21
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
General, Plastic Surgery (SU)
Clearance Type
Traditional
Third Party Flag
N
Date Received
2018-04-25

Related Establishments / Registrations

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