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FDA 510(k)

CTU676 DEVICE

K-Number: K073013 · 2007-11-21

ApplicantCompression Technologies Unlimited, Inc.
Decision Date2007-11-21
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

CTU676 DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Compression Technologies Unlimited, Inc.. It received FDA 510(k) clearance on 2007-11-21 under 510(k) number K073013. 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 CTU676 DEVICE?

CTU676 DEVICE is a medical device that received FDA 510(k) clearance on 2007-11-21. The listed applicant is Compression Technologies Unlimited, Inc.. The 510(k) number is K073013.

When did CTU676 DEVICE receive FDA 510(k) clearance?

CTU676 DEVICE received FDA 510(k) clearance on 2007-11-21, under 510(k) number K073013.

Who is the listed applicant for CTU676 DEVICE?

The FDA 510(k) record lists Compression Technologies Unlimited, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CTU676 DEVICE?

The FDA product code for CTU676 DEVICE is JOW.

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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.

K261807Sequential Circulator (SC-4004-DL, SC-4008-DL)Bio Compression Systems, Inc.K254217AerloomEvolym, LLCK253555Flexitouch® 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.

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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