Braebon Medical Corp. is one of 569 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Braebon Medical Corp. - FDA 510(k) Cleared Devices
Recent clearances: MEDIBYTE, MODEL MP8, MEDIPALM-20, ULTIMA SNORING MIKE, MODEL 0540
8
Total
8
Cleared
0
Denied
Braebon Medical Corp. has 8 FDA 510(k) cleared medical devices. Based in Carp, Ontario, CA.
Historical record: 8 cleared submissions from 1998 to 2006. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Braebon Medical Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Entela, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Braebon Medical Corp.
8 devices
Cleared
Sep 06, 2006
MEDIBYTE, MODEL MP8
Anesthesiology
76d
Cleared
May 01, 2003
MEDIPALM-20
Neurology
15d
Cleared
Aug 07, 2002
ULTIMA SNORING MIKE, MODEL 0540
Anesthesiology
189d
Cleared
Aug 25, 2000
ULTIMA SMARTBELT, MODEL 0560
Anesthesiology
78d
Cleared
Dec 30, 1998
ULTIMA AIRFLOW PRESSURE SENSOR
Anesthesiology
19d
Cleared
Oct 05, 1998
ULTIMA AIRFLOW SENSOR, 0510
Anesthesiology
166d
Cleared
Sep 11, 1998
ULTIMA RESPIRATORY EFFORT SENSOR MODELS 0520 AND 0522
Anesthesiology
80d
Cleared
Aug 20, 1998
ULTIMA BODY POSITION SENSOR
Neurology
77d