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FDA 510(k)

DE VO/44 OXYGEN CONCENTRATOR #444

K-Number: K830174 · 1983-02-17

Decision Date1983-02-17
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DE VO/44 OXYGEN CONCENTRATOR #444 is the device name listed in this FDA 510(k) record. The listed applicant is The Devilbiss Co.. It received FDA 510(k) clearance on 1983-02-17 under 510(k) number K830174. 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 DE VO/44 OXYGEN CONCENTRATOR #444?

DE VO/44 OXYGEN CONCENTRATOR #444 is a medical device that received FDA 510(k) clearance on 1983-02-17. The listed applicant is The Devilbiss Co.. The 510(k) number is K830174.

When did DE VO/44 OXYGEN CONCENTRATOR #444 receive FDA 510(k) clearance?

DE VO/44 OXYGEN CONCENTRATOR #444 received FDA 510(k) clearance on 1983-02-17, under 510(k) number K830174.

Who is the listed applicant for DE VO/44 OXYGEN CONCENTRATOR #444?

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

What is the FDA product code for DE VO/44 OXYGEN CONCENTRATOR #444?

The FDA product code for DE VO/44 OXYGEN CONCENTRATOR #444 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 The Devilbiss Co. 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 12 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

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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