The following data is part of a premarket notification filed by Maine Standards Company Llc with the FDA for Validate D-dimer Calibration Verification / Linearity Test Kit.
Device ID | K170864 |
510k Number | K170864 |
Device Name: | VALIDATE D-Dimer Calibration Verification / Linearity Test Kit |
Classification | Plasma, Coagulation Control |
Applicant | Maine Standards Company LLC 221 US Route 1 Cumberland Foreside, ME 04110 |
Contact | James Champlin |
Correspondent | James Champlin Maine Standards Company LLC 221 US Route 1 Cumberland Foreside, ME 04110 |
Product Code | GGN |
CFR Regulation Number | 864.5425 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-03-23 |
Decision Date | 2017-06-21 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00859110005081 | K170864 | 000 |