Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3021169869

FEI Number

3021169869

Entity Name

DIAGNOSTIC SUPPORT SERVICES

City/State/Country

Aurora, IL, US

Establishment Address

3557 Butterfield Rd Ste 105, Aurora, IL 60502, US

Establishment Type(s)

Repack or Relabel Medical Device

Owner / Operator

Diagnostic Support Services (Owner Number: 10083259)

Owner / Operator Contact Address

3557 West Butterfield Rd, Suite 105, Aurora, IL 60502, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

EsoGuard

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
NNK	Container, Specimen Mailer And Storage, Non-Sterile	Pathology	Class 1	864.3250	2025-11-25

Official Correspondent

Howard Slutsky

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Diagnostic Support Services

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 3021169869. Last updated year: 2026. Please use registration number 3021169869 when referencing this establishment in official correspondence.