510(k) K163498

VALIDATE Heparin Calibration Verification/Linearity Test Kit by Maine Standards Company, LLC — Product Code GGN

K163498 is an FDA 510(k) premarket notification submitted by Maine Standards Company, LLC for the device "VALIDATE Heparin Calibration Verification/Linearity Test Kit". The FDA issued a decision of Substantially Equivalent on March 16, 2017. The device falls under product code GGN (Plasma, Coagulation Control), a Class II device regulated under 21 CFR 864.5425. Maine Standards Company, LLC has at least 6 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 16, 2017
Date Received
December 13, 2016
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plasma, Coagulation Control
Device Class
Class II
Regulation Number
864.5425
Review Panel
HE
Submission Type