Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VASO PRESS DVT FOOT GARMENT #VP 520

K-Number: K003828 · 2001-05-18

ApplicantBritt Corp., Inc.
Decision Date2001-05-18
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASO PRESS DVT FOOT GARMENT #VP 520 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 2001-05-18 under 510(k) number K003828. 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 FOOT GARMENT #VP 520?

VASO PRESS DVT FOOT GARMENT #VP 520 is a medical device that received FDA 510(k) clearance on 2001-05-18. The listed applicant is Britt Corp., Inc.. The 510(k) number is K003828.

When did VASO PRESS DVT FOOT GARMENT #VP 520 receive FDA 510(k) clearance?

VASO PRESS DVT FOOT GARMENT #VP 520 received FDA 510(k) clearance on 2001-05-18, under 510(k) number K003828.

Who is the listed applicant for VASO PRESS DVT FOOT GARMENT #VP 520?

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 FOOT GARMENT #VP 520?

The FDA product code for VASO PRESS DVT FOOT GARMENT #VP 520 is JOW.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K991038VASO PRESS DVT SYSTEM, MODELS VP500, VP501K974393VASO 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

View all 17 devices →

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.

↑