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)

MODIFICATION TO VENTURE IHO 100 COMPLETE HOME OXYGEN SYSTEM

K-Number: K983777 · 1998-12-18

ApplicantInvacare Corp.
Decision Date1998-12-18
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO VENTURE IHO 100 COMPLETE HOME OXYGEN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1998-12-18 under 510(k) number K983777. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO VENTURE IHO 100 COMPLETE HOME OXYGEN SYSTEM?

MODIFICATION TO VENTURE IHO 100 COMPLETE HOME OXYGEN SYSTEM is a medical device that received FDA 510(k) clearance on 1998-12-18. The listed applicant is Invacare Corp.. The 510(k) number is K983777.

When did MODIFICATION TO VENTURE IHO 100 COMPLETE HOME OXYGEN SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO VENTURE IHO 100 COMPLETE HOME OXYGEN SYSTEM received FDA 510(k) clearance on 1998-12-18, under 510(k) number K983777.

Who is the listed applicant for MODIFICATION TO VENTURE IHO 100 COMPLETE HOME OXYGEN SYSTEM?

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

What is the FDA product code for MODIFICATION TO VENTURE IHO 100 COMPLETE HOME OXYGEN SYSTEM?

The FDA product code for MODIFICATION TO VENTURE IHO 100 COMPLETE HOME OXYGEN SYSTEM is CAW.

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 Invacare Corp. 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.

K071928THE INVACARE FLYER, MODEL IPC 100K070321TWILIGHT FULL FACE MASKK062402EASYSTAND EVOLVK061874INVACARE'S TWILIGHT II NASAL MASKSK033819INVACARE 3G TARSYSK031176INVACARE POLARIS EX HEATED HUMIDIFIER, MODEL ISP4000

View all 111 devices →

Related Devices (Code: CAW)

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.

K254289Portable Oxygen Concentrator (OX-1A-E, OX-1B)Oxytek Medical Technology Co., Ltd.K260171Portable Oxygen Concentrator (PO1 5B, PO1 6B)BMC Medical Co., Ltd.K252399Portable Oxygen ConcentratorHonsun (Nantong) Co., Ltd.K252965Oxygen Concentrator (OX-5A, OX-5C)Oxytek Medical Technology Co., Ltd.K252407OxyGo Portable Oxygen Concentrator (1400-7000)Mv Life, LLCK253549DeVilbiss 5 Liter Oxygen Concentrator (555)Devilbiss Healthcare, LLC

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.

↑