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

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

K Number: K170869 · Decision Apr 21, 2017
Classifications
1
FEI Numbers
839
Registration Numbers
839
Same Product Code
2251
Applicant Total
50
Review Days
29

Basic Information

Device Name
LigaSure Maryland Jaw Sealer/Divider One-step Sealing, Nano-coated
K Number
K170869
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Covidien
Date Received
March 23, 2017
Decision Date
April 21, 2017
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GEI), ordered by most recent decision date.

View all

Other Clearances by Covidien

K Number Device Name
K241486 Sofsilk™ Coated Braided Silk Suture
K240077 Mon-a-Therm™ General Purpose Temperature Probe 400TM (90050, 90044)
K231934 GIA™ Stapler with Tri-Staple™ Technology
K231240 MaxTack™ Motorized Fixation Device
K223130 Shiley™ Pediatric Oral/Nasal Endotracheal Tube with TaperGuard™ Cuff, Non DEHP (86125, 86130, 86135, 86140, 86145, 86150, 86155, 86160)
K232126 EEA™Circular Stapler with Tri-Staple™ Technology and OrVil™ Transoral Circular Stapler Anvil
K231491 TA™ Stapler and Loading Unit with DST Series™ Technology
K221629 Tri-Staple™ 2.0 Black Circular Reloads (for use with Signia™ Circular Adapters)
K221771 EEA Circular Stapler with Tri-Staple Technology
K222641 Signia™ Small Diameter Reloads Including Regular (Round) Tip Version
Search all 50 clearances from Covidien →