Maine Standards Company, LLC - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Maine Standards Company, LLC has 7 FDA 510(k) cleared medical devices. Based in Windham, US.
Historical record: 7 cleared submissions from 2011 to 2017. Primary specialty: Hematology.
Browse the FDA 510(k) cleared devices submitted by Maine Standards Company, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Maine Standards Company, LLC
7 devices
Cleared
Jun 21, 2017
VALIDATE D-Dimer Calibration Verification / Linearity Test Kit
Hematology
90d
Cleared
Mar 16, 2017
VALIDATE Heparin Calibration Verification/Linearity Test Kit
Hematology
93d
Cleared
Jan 05, 2017
VALIDATE® D-Dimer Calibration Verification/ Linearity Test Kit
Hematology
99d
Cleared
Jun 03, 2016
VALIDATE D-Dimer Calibration Verification/Linearity Test Kit
Hematology
240d
Cleared
Apr 30, 2015
VALIDATE Anemia Calibration Verification/ Linearity Test Kit
Chemistry
198d
Cleared
Feb 05, 2014
VALIDATE FERRITIN CALIBRATION VERIFICATION/ LINEARITY TEST KIT
Chemistry
78d
Cleared
Jul 05, 2011
VALIDATE (R) GC3 CALIBRATION VERIFICATION / LINEARITY TEST KIT
Chemistry
97d