# ACCUMETRA

FEI: 3014498605
Status: Active
Establishment types: Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Owner/operator: Accumetra (#10057556)

Address: Accumetra, 7 Corporate Drive, Clifton Park, NY, US



## Products

Total registered: 1
Top product codes: LHO
Regulation §: 892.1940

Proprietary names: CTLX1

## Source

- openFDA: https://api.fda.gov/device/registrationlisting.json?search=registration.fei_number:%223014498605%22
- FDA Registration Lookup: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm?lid=3014498605