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FDA 510(k)

DVT Motion Pneumatic Compression Device

K-Number: K232270 · 2024-03-06

ApplicantKoge Micro Tech Co., Ltd.
Decision Date2024-03-06
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

DVT Motion Pneumatic Compression Device is a medical device manufactured by Koge Micro Tech Co., Ltd.. It received FDA 510(k) clearance on 2024-03-06 under approval number K232270. The device is classified under product code JOW. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DVT Motion Pneumatic Compression Device?

DVT Motion Pneumatic Compression Device is a medical device that received FDA 510(k) clearance on 2024-03-06. It is manufactured by Koge Micro Tech Co., Ltd.. The 510(k) number is K232270.

When was DVT Motion Pneumatic Compression Device approved by the FDA?

DVT Motion Pneumatic Compression Device received FDA 510(k) clearance on 2024-03-06, under approval number K232270.

What company makes DVT Motion Pneumatic Compression Device?

DVT Motion Pneumatic Compression Device is manufactured by Koge Micro Tech Co., Ltd..

What is the FDA product code for DVT Motion Pneumatic Compression Device?

The FDA product code for DVT Motion Pneumatic Compression Device is JOW.

Related Clinical Trials

NCT07613931 Evaluate Advanced Pneumatic Compression Device With Revised Compression Programming for Lymphedema Treatment NOT_YET_RECRUITING NCT01961557 Evaluating a New Knee-Ankle-Foot Brace to Improve Gait in Children With Movement Disorders COMPLETED NCT06192134 Continuous Passive Motion Device for Children With Arthrogryposis NOT_YET_RECRUITING NCT07603531 Assessment of the Efficacy of the Dynamic Decongestive System in the Maintenance Phase of Lower Limb Lymphedema NOT_YET_RECRUITING NCT07305870 Sequential Compression Device in Distributive Peripheral Edema and Hemodynamic Stability Among Patients in Critical Care Units ENROLLING_BY_INVITATION NCT07600489 A Randomized Non-Inferiority Study of Mepi™ Press 2 vs UrgoK2® for Compression Therapy in Venous Leg Ulcers NOT_YET_RECRUITING

Related PubMed Literature

PMID: 40487675 Antiemetic effect of acupressure wristbands for GLP-1 medication associated nausea. Obesity pillars (2025)

Related Devices (Code: JOW)

K163055Reprocessed Kendall SCD Express Foot CuffCovidien K160180Intermittent Pneumatic Compression systemDaesung Maref Co., Ltd. K161105Reprocessed Compression GarmentsCovidien K160431ActiveCare HomeMedical Compression Systems (Dbn) , Ltd. K161346NormaTec PCD-T and PCD-BNormaTec Industries, LP K161209Cirona 6400Devon Medical Products

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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