Mesa Laboratories, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Mesa Laboratories, Inc. has 9 FDA 510(k) cleared medical devices. Based in Lakewood, US.
Historical record: 9 cleared submissions from 2004 to 2020. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Mesa Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Mesa Laboratories, Inc.
9 devices
Cleared
Sep 02, 2020
SmartHDM-510 System
Gastroenterology & Urology
65d
Cleared
Aug 05, 2019
TDS Standard Solution
Gastroenterology & Urology
61d
Cleared
Sep 21, 2015
Phoenix XL Dialysate Meter
Gastroenterology & Urology
192d
Cleared
Dec 03, 2014
STERRAD CYCLESURE 24 PLUS BIOLOGICAL INDICATOR
General Hospital
271d
Cleared
Apr 18, 2013
COMINED STANDARD SOLUTION
Gastroenterology & Urology
93d
Cleared
Mar 26, 2013
SMART-WELL INCUBATOR
General Hospital
232d
Cleared
Jan 30, 2012
SMART READ EZTEST STEAM
General Hospital
200d
Cleared
May 05, 2005
90XL INSTRUMENTATION SYSTEM
Gastroenterology & Urology
35d
Cleared
Feb 27, 2004
CONDUCTIVITY/TDS CALIBRATOR SOLUTION
Gastroenterology & Urology
134d