MOBILAIRE III AND V MODEL IRC 301 AND 501 OXY. CON
K-Number: K904087 · 1990-10-26
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Device Summary
Frequently Asked Questions
What is the MOBILAIRE III AND V MODEL IRC 301 AND 501 OXY. CON?
MOBILAIRE III AND V MODEL IRC 301 AND 501 OXY. CON is a medical device that received FDA 510(k) clearance on 1990-10-26. The listed applicant is Invacare Corp.. The 510(k) number is K904087.
When did MOBILAIRE III AND V MODEL IRC 301 AND 501 OXY. CON receive FDA 510(k) clearance?
MOBILAIRE III AND V MODEL IRC 301 AND 501 OXY. CON received FDA 510(k) clearance on 1990-10-26, under 510(k) number K904087.
Who is the listed applicant for MOBILAIRE III AND V MODEL IRC 301 AND 501 OXY. CON?
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 MOBILAIRE III AND V MODEL IRC 301 AND 501 OXY. CON?
The FDA product code for MOBILAIRE III AND V MODEL IRC 301 AND 501 OXY. CON 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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