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Ge Lunar Visceral Fat Software

by Ge Medical Systems Ultrasound and Primary Care Dia FDA registration: United States 510(k)

510(k) K103730 Product code KGI

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK103730 Date6 May 2011ClearedStatusActive

Coverage

1 jurisdiction

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  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

United States — FDA 510(k) Active

Recalls: none on record (FDA, checked 22 Oct 2026)

Specification

510(k) · synced 22 Oct 2026

510(k) Number
FDA Product Code
KGI
Device Class
Class II
Regulation
21 CFR Part 892.1170
Advisory Committee
Radiology
FDA Decision
SESE Substantially Equivalent

Other devices from Ge Medical Systems Ultrasound and Primary Care Dia

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Properties & raw data

Show properties, registry sources and raw records

Sources (1)

  • FDA 510(k) K103730 24 fields · synced 22 Oct 2026