Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Applications Submitted by JAMES W CHAMPLIN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170864
03/23/2017
VALIDATE D-Dimer Calibration Verification / Linearity Test Kit
Maine Standards Company LLC
K162705
09/28/2016
VALIDATE« D-Dimer Calibration Verification/ Linearity Test Kit
MAINE STANDARDS COMPANY LLC
K152961
10/07/2015
VALIDATE D-Dimer Calibration Verification/Linearity Test Kit
MAINE STANDARDS COMPANY LLC
K142964
10/14/2014
VALIDATE Anemia Calibration Verification/ Linearity Test Kit
MAINE STANDARDS COMPANY, LLC
K163498
12/13/2016
VALIDATE Heparin Calibration Verification/Linearity Test Kit
MAINE STANDARDS COMPANY, LLC
K123127
10/04/2012
VALIDATE PSA CALIBRATION VERIFICATION/ LINEARITY TEST KIT MODEL 406
MAINE STANDARDS CO.
K133550
11/19/2013
VALIDATE FERRITIN CALIBRATION VERIFICATION/ LINEARITY TEST KIT
MAINE STANDARDS COMPANY LLC
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact