# LGC Clinical Diagnostics, Inc.

FEI: 1220394
Status: Active
Establishment types: Manufacture Medical Device
Owner/operator: LGC Clinical Diagnostics, Inc. (#9041170)

Address: 37 Birch St, Milford, MA, US



## Products

Total registered: 1
Top product codes: JJY
Regulation §: 862.1660

Proprietary names: VALIDATE Body Fluids 2 Calibration Verification/Linearity Test Kit, product code: 206ro, VALIDATE UC5 Calibration Verification/Linearity Test Kit, product code: 705ab, VALIDATE UC1 Calibration Verification/Linearity Test Kit, product code: 701ab, 701re, 701sa, VALIDATE Body Fluids Calibration Verification/Linearity Test Kit, product codes: 205bf, 205ro, VALIDATE Fertility 3 Calibration Verification/Linearity Test Kit, product code: 505ro, VALIDATE Fertility 1 Calibration Verification/Linearity Test Kit, product code: 502ab, 502re, VALIDATE THY2 Hormone Calibration Verification/Linearity Test Kit, product code:908bc, VALIDATE Diabetes Calibration Verification/Linearity Test Kit, product code: 204ro, VALIDATE® CM2 Calibration Verification / Linearity Test Set (Product Code 402pf), VALIDATE IBC Calibration Verification/Linearity Test Kit, product codes: 203ro, 203sd, 203vt

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%221220394%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=1220394