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Ge Medical Systems Lunar

FDA Regulatory Profile

Ge Medical Systems Lunar appears in FDA public data with 0 recalls, 2 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 27, 2012.

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K113286ENCORE 14 SOFTWARE RELEASE FOR THE GE LUNAR DXA BONE DENSITOMETERSApril 27, 2012
K071570GE LUNAR BODY COMPOSITION SOFTWAREJune 27, 2007

FDA data resources