Baylis Medical Co., Inc. - FDA 510(k) Cleared Devices
28
Total
28
Cleared
0
Denied
Baylis Medical Co., Inc. has 28 FDA 510(k) cleared medical devices. Based in Mississauga, CA.
Historical record: 28 cleared submissions from 1998 to 2013.
Browse the FDA 510(k) cleared devices submitted by Baylis Medical Co., Inc. Filter by specialty or product code using the sidebar.
28 devices
Cleared
Jan 24, 2013
SUREFLEX STEERABLE GUIDING SHEATH KIT
Cardiovascular
122d
Cleared
Mar 13, 2012
OSTEOCOOL (TM) RF ABLATION SYSTEM
General & Plastic Surgery
286d
Cleared
Apr 01, 2011
TORFLEX TRANSSEPTAL GUIDING SHEATH
Cardiovascular
178d
Cleared
Feb 23, 2011
INDISCAL DIGITAL MANOMETER
General Hospital
203d
Cleared
Aug 10, 2010
DUOCOOL PAIN MANAGEMENT PROBE, MODEL OSP-17-180-20
Neurology
85d
Cleared
Jul 28, 2010
POWERWIRE RADIOFREQUENCY GUIDEWIRE
Cardiovascular
49d
Cleared
Jul 16, 2010
LEV-OR DILATION CATHETER OTW
Cardiovascular
86d
Cleared
Nov 17, 2009
INDISCAL ASPIRATION DEVICE AND ACCESSORIES
Orthopedic
60d
Cleared
Oct 16, 2009
PAIN MANAGEMENT OPTIMA, MODEL PMO21-100-05, PMO20-100-10CS, PMO20-145-10CS
Neurology
73d
Cleared
May 28, 2008
NRG TRANSSEPTAL NEEDLE
Cardiovascular
183d
Cleared
Dec 19, 2007
BAYLIS PAIN MANAGEMENT GENERATOR-TD, MODELS: PMG-115-TD AND PMG-230-TD
General & Plastic Surgery
106d
Cleared
Jul 19, 2007
BAYLIS PAIN MANAGEMENT SINGLE-USE PROBE
Neurology
22d