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FDA 510(k)

MOBILAIRE II(P2A) OXYGEN CONCENTRATOR

K-Number: K851438 · 1985-07-29

Decision Date1985-07-29
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MOBILAIRE II(P2A) OXYGEN CONCENTRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1985-07-29 under 510(k) number K851438. 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 MOBILAIRE II(P2A) OXYGEN CONCENTRATOR?

MOBILAIRE II(P2A) OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1985-07-29. The listed applicant is Invacare Corp.. The 510(k) number is K851438.

When did MOBILAIRE II(P2A) OXYGEN CONCENTRATOR receive FDA 510(k) clearance?

MOBILAIRE II(P2A) OXYGEN CONCENTRATOR received FDA 510(k) clearance on 1985-07-29, under 510(k) number K851438.

Who is the listed applicant for MOBILAIRE II(P2A) OXYGEN CONCENTRATOR?

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 II(P2A) OXYGEN CONCENTRATOR?

The FDA product code for MOBILAIRE II(P2A) OXYGEN CONCENTRATOR 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.

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.

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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