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Braebon Medical Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K061764MEDIBYTE, MODEL MP8September 6, 2006
K031202MEDIPALM-20May 1, 2003
K020312ULTIMA SNORING MIKE, MODEL 0540August 7, 2002
K001743ULTIMA SMARTBELT, MODEL 0560August 25, 2000
K984431ULTIMA AIRFLOW PRESSURE SENSORDecember 30, 1998
K981445ULTIMA AIRFLOW SENSOR, 0510October 5, 1998
K982216ULTIMA RESPIRATORY EFFORT SENSOR MODELS 0520 AND 0522September 11, 1998
K981969ULTIMA BODY POSITION SENSORAugust 20, 1998