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FDA 510(k)

VMT SYSTEM

K-Number: K971549 · 1998-10-05

ApplicantTarget Health, Inc.
Decision Date1998-10-05
Product CodeLXV
DecisionSubstantially Equivalent

Device Summary

VMT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Target Health, Inc.. It received FDA 510(k) clearance on 1998-10-05 under 510(k) number K971549. The device is classified under product code LXV. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VMT SYSTEM?

VMT SYSTEM is a medical device that received FDA 510(k) clearance on 1998-10-05. The listed applicant is Target Health, Inc.. The 510(k) number is K971549.

When did VMT SYSTEM receive FDA 510(k) clearance?

VMT SYSTEM received FDA 510(k) clearance on 1998-10-05, under 510(k) number K971549.

Who is the listed applicant for VMT SYSTEM?

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

What is the FDA product code for VMT SYSTEM?

The FDA product code for VMT SYSTEM is LXV.

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 Target Health, 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.

K973271SKAR-KAREK971009SCAR CARE

Related Devices (Code: LXV)

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.

K220231GyroStimUltrathera Technologies, Inc.K200529OrionInteracoustics A/SK192652TRVInteracoustics A/SK183661ClearEdge Balance SystemQuadrant BiosciencesK190735EQ BalanceUpright Science, Inc.K173669K-D BalanceKing-Devick Technologies, Inc.

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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