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ECHELON LINEAR™ 60 mm Cutter (GLC60) +8 more models

FDA 510(k)

Class II (US FDA 510(k))

510(k) K223760

by Ethicon Endo-Surgery

Identifiers

510(k) Number
K223760 FDA 510(k)
FDA Product Code
GDW FDA 510(k)
Models / Variants
ECHELON LINEAR™ 60 mm Cutter (GLC60) FDA 510(k)
ECHELON LINEAR™ 80mm Cutter (GLC80) FDA 510(k)
ECHELON LINEAR™ 100 mm Cutter (GLC100) FDA 510(k)
ECHELON LINEAR™ Cutters 60mm Blue Reload (GLCR60B) FDA 510(k)
ECHELON LINEAR™ Cutters 60mm Green Reload (GLCR60G) FDA 510(k)
ECHELON LINEAR™ Cutters 80mm Blue Reload (GLCR80B) FDA 510(k)
ECHELON LINEAR™ Cutters 80mm Green Reload (GLCR80G) FDA 510(k)
ECHELON LINEAR™ Cutters 100mm Blue Reload (GLCR100B) FDA 510(k)
ECHELON LINEAR™ Cutters 100mm Green Reload (GLCR100G) FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 878.4750 FDA 510(k)
Regulation Number
878.4750 FDA 510(k)
Advisory Committee
General, Plastic Surgery FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

ECHELON LINEAR™ 60 mm Cutter (GLC60) +8 more models by Ethicon Endo-Surgery — Class II — FDA_510K — listed in FDA 510(k) — 9 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Ethicon Endo-Surgery

Sources (1)

  • FDA 510(k) K223760 24 fields · synced Jun 19, 2026