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ULTRACISION HARMONIC SCALPEL COAGULATING SHEARS - Cs231

FDA 510(k)

Class II (US FDA 510(k))

510(k) K002981

by Ethicon Endo-Surgery, Inc.

Identifiers

510(k) Number
K002981 FDA 510(k)
FDA Product Code
GEI FDA 510(k)
Models / Variants
Lcsc5 FDA 510(k)
Lcsc1 FDA 510(k)
Cs23c FDA 510(k)
Cs231 FDA 510(k)
Cs14c FDA 510(k)
Cs141 FDA 510(k)
Lcsb5 FDA 510(k)
Lcsk5 FDA 510(k)
Lcs15 FDA 510(k)
Lcs16 FDA 510(k)
Cs150 FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 878.4400 FDA 510(k)
Regulation Number
878.4400 FDA 510(k)
Advisory Committee
General, Plastic Surgery FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

ULTRACISION HARMONIC SCALPEL COAGULATING SHEARS - Cs231 by Ethicon Endo-Surgery, Inc. — Class II — FDA_510K — listed in FDA 510(k) — 11 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Ethicon Endo-Surgery, Inc.

Sources (1)

  • FDA 510(k) K002981 24 fields · synced Jun 18, 2026