Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

2000010846

FEI Number

2000010846

Entity Name

MEDICORE CO. LTD.

City/State/Country

Seongnam-si Gyeonggi, KR

Establishment Address

No. 801 803, Joonganginnotech, 148, Sagimakgolro,, Jungwon-gu,, Seongnam-si Gyeonggi 13207, KR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

MEDICORE CO. LTD. (Owner Number: 10025245)

Owner / Operator Contact Address

No.801-803, Joonganginnotech, 148, Sagimakgolro, Jungwon-gu, Seongnam, KR-41 13207, KR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

K110374

PMA Number

N/A

All Registered Proprietary Names

SA-3000P Max Pulse

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
JOM	Plethysmograph, Photoelectric, Pneumatic Or Hydraulic	Cardiovascular	Class 2	870.2780	2008-03-26
JOM	Plethysmograph, Photoelectric, Pneumatic Or Hydraulic	Cardiovascular	Class 2	870.2780	2012-02-02

Official Correspondent

Byung-kuk YOO

US Agent Details

Trina Tew Email: waynebaumgarten@gmail.com Phone: (216) 6011050

Related Public Records

Same Entity

MEDICORE CO. LTD.

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 2000010846. Last updated year: 2026. Please use registration number 2000010846 when referencing this establishment in official correspondence.