Galix Biomedical Instrumentation, Inc.

FDA Regulatory Profile

Galix Biomedical Instrumentation, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 3 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 9, 2010.

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
3
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K0928533 CHANNEL DIGITAL AMBULATORY ECG RECORDER MODEL GALIX GBI-3SMJuly 9, 2010
K051163GALIX ECG PROFESSIONAL STATIONJanuary 31, 2006
K030145GALIX WINTERSeptember 17, 2003
K023080GALIX PACESTARJune 11, 2003
K992706GALIX GBI -3S-LPMarch 15, 2001
K9716703 CHANNEL DIGITAL AMBULATORY ECG RECORDERJanuary 29, 1998