VENTURE HOMEFILL II WITH OXYGEN CONSERVER
K-Number: K021685 · 2002-07-23
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Device Summary
Frequently Asked Questions
What is the VENTURE HOMEFILL II WITH OXYGEN CONSERVER?
VENTURE HOMEFILL II WITH OXYGEN CONSERVER is a medical device that received FDA 510(k) clearance on 2002-07-23. The listed applicant is Invacare Corp.. The 510(k) number is K021685.
When did VENTURE HOMEFILL II WITH OXYGEN CONSERVER receive FDA 510(k) clearance?
VENTURE HOMEFILL II WITH OXYGEN CONSERVER received FDA 510(k) clearance on 2002-07-23, under 510(k) number K021685.
Who is the listed applicant for VENTURE HOMEFILL II WITH OXYGEN CONSERVER?
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 VENTURE HOMEFILL II WITH OXYGEN CONSERVER?
The FDA product code for VENTURE HOMEFILL II WITH OXYGEN CONSERVER 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.
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.
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.
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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