Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014498605

FEI Number

3014498605

Entity Name

ACCUMETRA

City/State/Country

Clifton Park, NY, US

Establishment Address

Accumetra, 7 Corporate Drive, Clifton Park, NY 12065, US

Establishment Type(s)

Manufacture Medical Device,Complaint File Establishment per 21 CFR 820.198

Owner / Operator

Accumetra (Owner Number: 10057556)

Owner / Operator Contact Address

Accumetra, LLC, 7 Corporate Drive, Clifton Park, NY 12065, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

CTLX1

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LHO	Instrument, Quality-Assurance, Radiologic	Radiology	Class 1	892.1940	2018-04-24

Official Correspondent

Ricardo Avila

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Accumetra

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014498605. Last updated year: 2026. Please use registration number 3014498605 when referencing this establishment in official correspondence.