EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG— 510(k) K242770

Name: FDA 510(k) clearance K242770
Creator: U.S. Food and Drug Administration
Published: 2025-03-20

Substantially Equivalent

DRTECH Corporation

FDA 510(k) clearance K242770 for EXPD 114; EXPD 114G; EXPD 114P; EXPD 114PG, Substantially Equivalent on 2025-03-20. Applicant: DRTECH Corporation. Device class: 2.

Clearance details

Applicant: DRTECH Corporation
Product code: Code MQB
Device class: Class 2
Regulation: 21 CFR 892.1680
Advisory panel: Radiology
Date received: 2024-09-13
Decision date: 2025-03-20
Decision: Substantially Equivalent
Clearance type: Special
Location: Jungwon-Gu, Seongnam-Si, 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.