The following data is part of a premarket notification filed by Maine Standards Co. with the FDA for Validate Thyroid Calibration Verification / Linearity Test Set, Model 901.
Device ID | K062501 |
510k Number | K062501 |
Device Name: | VALIDATE THYROID CALIBRATION VERIFICATION / LINEARITY TEST SET, MODEL 901 |
Classification | Single (specified) Analyte Controls (assayed And Unassayed) |
Applicant | MAINE STANDARDS CO. 765 ROOSEVELT TRAIL Windham, ME 04062 -5365 |
Contact | Holly Cressman |
Correspondent | Holly Cressman MAINE STANDARDS CO. 765 ROOSEVELT TRAIL Windham, ME 04062 -5365 |
Product Code | JJX |
CFR Regulation Number | 862.1660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-08-25 |
Decision Date | 2006-09-29 |
Summary: | summary |