FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

LigaSure Advance Monopolar Tip Laparoscopic Sealer/Divider, Pistol Grip

K Number: K150835 · Decision Oct 15, 2015
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
130
Review Days
199

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Basic Information

Device Name
LigaSure Advance Monopolar Tip Laparoscopic Sealer/Divider, Pistol Grip
K Number
K150835
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Covidien
Date Received
March 30, 2015
Decision Date
October 15, 2015
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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