Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

9615335

FEI Number

3002806858

Entity Name

Datrend Systems Inc

City/State/Country

RICHMOND British Columbia, CA

Establishment Address

4020 Viking Way, Unit 130, RICHMOND British Columbia V6V 2L4, CA

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

Datrend Systems Inc (Owner Number: 9032342)

Owner / Operator Contact Address

4020 Viking Way, Unit 130, RICHMOND, CA-BC V6V 2L4, CA

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K062099

PMA Number

N/A

All Registered Proprietary Names

Phase3 Defibrillator/Pacer Analyzer

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
DRL	Tester, Defibrillator	Cardiovascular	Class 2	870.5325	2008-11-04

Official Correspondent

RON EVANS

US Agent Details

Dave Heiselt Business: QRS Solutions Email: dave@qrs-solutions.com Phone: (951) 4882044

Related Public Records

Same Entity

Datrend Systems Inc

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 9615335. Last updated year: 2026. Please use registration number 9615335 when referencing this establishment in official correspondence.