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

GE LUNAR FEMUR STRENGTH SOFTWARE

K Number: K072664 · Decision Nov 21, 2008
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
146
Applicant Total
7
Review Days
428

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
GE LUNAR FEMUR STRENGTH SOFTWARE
K Number
K072664
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1170
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Ge Medical Systems Ultrasound and Primary Care Dia
Date Received
September 20, 2007
Decision Date
November 21, 2008
Product Code
KGI
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
KGI Densitometer, Bone

Similar 510(k) Clearances

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

View all

Other Clearances by Ge Medical Systems Ultrasound and Primary Care Dia

K Number Device Name
K103730 GE LUNAR VISCERAL FAT SOFTWARE
K082185 GE LOGIQ E9 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS 5205000, 5205000-2
K073408 GE LOGIQ BT08 DIAGNOSTIC ULTRASOUND SYSTEM
K072439 GE LUNAR DPX & PRODIGY SERIES DEXA BONE DENSITOMETERS WITH MOBILE KIT
K052581 LUNAR IDXA
K041813 GE LOGIQ 7 ULTRASOUND BT04