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FDA 510(k)

MODIFICATION TO INSPIRATION VENTILATOR SYSTEM

K-Number: K030341 · 2004-01-16

ApplicanteVent Medical, Ltd.
Decision Date2004-01-16
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO INSPIRATION VENTILATOR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is eVent Medical, Ltd.. It received FDA 510(k) clearance on 2004-01-16 under 510(k) number K030341. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO INSPIRATION VENTILATOR SYSTEM?

MODIFICATION TO INSPIRATION VENTILATOR SYSTEM is a medical device that received FDA 510(k) clearance on 2004-01-16. The listed applicant is eVent Medical, Ltd.. The 510(k) number is K030341.

When did MODIFICATION TO INSPIRATION VENTILATOR SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO INSPIRATION VENTILATOR SYSTEM received FDA 510(k) clearance on 2004-01-16, under 510(k) number K030341.

Who is the listed applicant for MODIFICATION TO INSPIRATION VENTILATOR SYSTEM?

The FDA 510(k) record lists eVent Medical, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFICATION TO INSPIRATION VENTILATOR SYSTEM?

The FDA product code for MODIFICATION TO INSPIRATION VENTILATOR SYSTEM is CBK.

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 eVent Medical, Ltd. 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.

K130178INSPIRATION VENTILATOR SYSTEM 5I/7IK051550INSPIRATION VENTILATOR SYSTEMK040220MEDICAL AIR COMPRESSORK021112INSPIRATION VENTILATOR SYSTEM

Related Devices (Code: CBK)

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.

K253647Evita (V800); Evita (V600)Draegerwerk AG & CO KgaaK252663Inbentus VersatileIconic Solutions by Murcia, SLK251888VPAP Pediatric Face MaskHsiner Co., Ltd.K232365Vivo 45 LSOconnell Regulatory Consultants, Inc.K252173F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size A (ONIV117A); F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size B (ONIV117B); F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size C (ONIV117C); F&P OptiNIV ONIV117-F Hospital Vented Full Face Mask with optional Expiratory Filter Compatible with Single-limb Circuits - Size A (ONIV117A-F); F&P OptiNIV ONIV117-F Hospital Vented FullFisher & Paykel Healthcare, Ltd.K243767SV600, SV800 VentilatorShenzhen Mindray Bio-Medical Electronics Co., 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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