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FDA 510(k)

COWBOY XV

K-Number: K981311 · 1999-04-23

ApplicantKci New Technologies, Inc.
Decision Date1999-04-23
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COWBOY XV is the device name listed in this FDA 510(k) record. The listed applicant is Kci New Technologies, Inc.. It received FDA 510(k) clearance on 1999-04-23 under 510(k) number K981311. 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 COWBOY XV?

COWBOY XV is a medical device that received FDA 510(k) clearance on 1999-04-23. The listed applicant is Kci New Technologies, Inc.. The 510(k) number is K981311.

When did COWBOY XV receive FDA 510(k) clearance?

COWBOY XV received FDA 510(k) clearance on 1999-04-23, under 510(k) number K981311.

Who is the listed applicant for COWBOY XV?

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

What is the FDA product code for COWBOY XV?

The FDA product code for COWBOY XV is JOW.

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Other records listing Kci New Technologies, Inc. as applicant

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.

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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

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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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