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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 the device name listed in this FDA 510(k) record. The listed applicant is Koge Micro Tech Co., Ltd.. It received FDA 510(k) clearance on 2024-03-06 under 510(k) 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. The listed applicant is Koge Micro Tech Co., Ltd.. The 510(k) number is K232270.

When did DVT Motion Pneumatic Compression Device receive FDA 510(k) clearance?

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

Who is the listed applicant for DVT Motion Pneumatic Compression Device?

The FDA 510(k) record lists Koge Micro Tech Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

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

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Related Devices (Code: JOW)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253555Flexitouch® Plus Advanced Pneumatic Compression SystemTactile MedicalK253386DVT GarmentVistar Medical Supplies Co., Ltd.K250242Compression Therapy Device (LGT-2202DVT)Guangzhou Longest Medical Technology Co., Ltd.K254267NanoPress 760A-BT (760A-BT)Mego Afek , Ltd.K250974Bio Arterial Deluxe (IC-BAP-DX)Bio Compression Systems, Inc.K250190Sequential Compression System (SCD600)Shenzhen Comen Medical Instruments Co.,Ltd

Official Source

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

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