Data / Medical devices / South Korea / Seoil Pacific Corp
Seoil Pacific Corp: FDA-registered device maker in Gimpo-si Gyeonggi, South Korea, 1 510(k) clearance
Seoil Pacific Corp is registered with the FDA (registration 3008700378) in Gimpo-si Gyeonggi, South Korea. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 21, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008700378
- Address
- 71, Hwanggeum 3-ro 7beon-gil Yangchon-eup, Gimpo-si Gyeonggi, South Korea, 10048
- Owner or operator
- SEOIL PACIFIC CORP (10043722)
- Roles
- Manufacturer
- First device listed
- March 14, 2013
- Registered through
- 2026
- Brand names listed
- Comfort Cough
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Device, Positive Pressure Breathing, Intermittent | NHJ | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| February 21, 2013 | K113549 | COMFORT COUGH | NHJ | Substantially Equivalent | Seoil Pacific Corp. | accessdata.fda.gov |
Compare with other makers
Updated February 21, 2013. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.