DVT Motion Pneumatic Compression Device— 510(k) K232270

Name: FDA 510(k) clearance K232270
Creator: U.S. Food and Drug Administration
Published: 2024-03-06

Substantially Equivalent

Koge Micro Tech Co., Ltd.

FDA 510(k) clearance K232270 for DVT Motion Pneumatic Compression Device, Substantially Equivalent on 2024-03-06. Applicant: Koge Micro Tech Co., Ltd.. Device class: 2.

Clearance details

Applicant: Koge Micro Tech Co., Ltd.
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 2023-07-31
Decision date: 2024-03-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Taipei, TW

Download summary PDF View on FDA.gov ↗

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