SEOIL PACIFIC CORP

FDA Device Registration & Listing · Gimpo-si Gyeonggi, KR · Registration 3008700378

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3008700378
FEI Number
3008700378
Entity Name
SEOIL PACIFIC CORP
City/State/Country
Gimpo-si Gyeonggi, KR
Establishment Address
71, Hwanggeum 3-ro 7beon-gil, Yangchon-eup, Gimpo-si Gyeonggi 10048, KR
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
SEOIL PACIFIC CORP (Owner Number: 10043722)
Owner / Operator Contact Address
Rm. 202-1, 515, 516, Ace High-End Tower, 5 Digital-ro 26-gil, Guro-gu, KR-11 08389, KR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

Comfort Cough

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NHJ Device, Positive Pressure Breathing, Intermittent Anesthesiology Class 2 868.5905 2013-03-14

Official Correspondent

Kye Cheol Kim

US Agent Details

Sunyoung Park Email: sypark@szukorea.com Phone: (682) 7729233

Related Public Records

Same Entity

SEOIL PACIFIC CORP
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008700378. Last updated year: 2026. Please use registration number 3008700378 when referencing this establishment in official correspondence.
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