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FDA 510(k)

VASO PRESS DVT SYSTEM, MODELS VP500, VP501

K-Number: K991038 · 2000-06-22

ApplicantBritt Corp., Inc.
Decision Date2000-06-22
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASO PRESS DVT SYSTEM, MODELS VP500, VP501 is the device name listed in this FDA 510(k) record. The listed applicant is Britt Corp., Inc.. It received FDA 510(k) clearance on 2000-06-22 under 510(k) number K991038. 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 VASO PRESS DVT SYSTEM, MODELS VP500, VP501?

VASO PRESS DVT SYSTEM, MODELS VP500, VP501 is a medical device that received FDA 510(k) clearance on 2000-06-22. The listed applicant is Britt Corp., Inc.. The 510(k) number is K991038.

When did VASO PRESS DVT SYSTEM, MODELS VP500, VP501 receive FDA 510(k) clearance?

VASO PRESS DVT SYSTEM, MODELS VP500, VP501 received FDA 510(k) clearance on 2000-06-22, under 510(k) number K991038.

Who is the listed applicant for VASO PRESS DVT SYSTEM, MODELS VP500, VP501?

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

What is the FDA product code for VASO PRESS DVT SYSTEM, MODELS VP500, VP501?

The FDA product code for VASO PRESS DVT SYSTEM, MODELS VP500, VP501 is JOW.

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Other records listing Britt Corp., 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.

K003828VASO PRESS DVT FOOT GARMENT #VP 520K974393VASO PRESS SYSTEMK860977MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATIONK860975MODEL 545-45 LASER FOR EAR, NOSE & THROATK860974MODEL 545-45 LASER FOR DERMA., POD., SURGICALK860277MODEL 525-25 WATT C02 LASER FOR EAR, NOSE & THROAT

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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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