Goyo Mouthpiece S— 510(k) K232238

Substantially Equivalent

Dimedikorea

FDA 510(k) clearance K232238 for Goyo Mouthpiece S, Substantially Equivalent on 2024-04-17. Applicant: Dimedikorea. Device class: Unclassified.

Clearance details

Applicant: Dimedikorea
Product code: Code OBR
Device class: Unclassified
Advisory panel: Unknown
Date received: 2023-07-28
Decision date: 2024-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Busan, KR

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.