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FDA 510(k)

ANGIO-PRESS LITE DVT Compression Device

K-Number: K173012 · 2018-05-10

ApplicantPegasus Medical Supply, Inc.
Decision Date2018-05-10
Product CodeJOW
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ANGIO-PRESS LITE DVT Compression Device is a medical device manufactured by Pegasus Medical Supply, Inc.. It received FDA 510(k) clearance on 2018-05-10 under approval number K173012. 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 ANGIO-PRESS LITE DVT Compression Device?

ANGIO-PRESS LITE DVT Compression Device is a medical device that received FDA 510(k) clearance on 2018-05-10. It is manufactured by Pegasus Medical Supply, Inc.. The 510(k) number is K173012.

When was ANGIO-PRESS LITE DVT Compression Device approved by the FDA?

ANGIO-PRESS LITE DVT Compression Device received FDA 510(k) clearance on 2018-05-10, under approval number K173012.

What company makes ANGIO-PRESS LITE DVT Compression Device?

ANGIO-PRESS LITE DVT Compression Device is manufactured by Pegasus Medical Supply, Inc..

What is the FDA product code for ANGIO-PRESS LITE DVT Compression Device?

The FDA product code for ANGIO-PRESS LITE DVT Compression Device is JOW.

Related Clinical Trials

NCT07613931 Evaluate Advanced Pneumatic Compression Device With Revised Compression Programming for Lymphedema Treatment NOT_YET_RECRUITING NCT07603531 Assessment of the Efficacy of the Dynamic Decongestive System in the Maintenance Phase of Lower Limb Lymphedema NOT_YET_RECRUITING NCT07305870 Sequential Compression Device in Distributive Peripheral Edema and Hemodynamic Stability Among Patients in Critical Care Units ENROLLING_BY_INVITATION NCT07600489 A Randomized Non-Inferiority Study of Mepi™ Press 2 vs UrgoK2® for Compression Therapy in Venous Leg Ulcers NOT_YET_RECRUITING NCT07573189 The Effects of Recovery Compression Boots on Blood Lactate Levels, Functional Movement, and Joint Ange of Motion in Collegiate Athletes. ACTIVE_NOT_RECRUITING NCT06911385 Augmenting Cerebral Blood Flow in Acute Ischemic Stroke NOT_YET_RECRUITING

Related PubMed Literature

PMID: 39981570 Variations in the Medical Device Authorization and Reimbursement Landscape: A Case Study of 2 Cardiovascular Devices Across 4 Countries. Circulation. Cardiovascular quality and outcomes (2025)

Related Devices (Code: JOW)

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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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