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FDA 510(k)

MAX 02 OXYGEN CONCENTRATOR

K-Number: K833500 · 1983-11-29

Decision Date1983-11-29
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MAX 02 OXYGEN CONCENTRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Mountain Medical Equipment, Inc.. It received FDA 510(k) clearance on 1983-11-29 under 510(k) number K833500. 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 MAX 02 OXYGEN CONCENTRATOR?

MAX 02 OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1983-11-29. The listed applicant is Mountain Medical Equipment, Inc.. The 510(k) number is K833500.

When did MAX 02 OXYGEN CONCENTRATOR receive FDA 510(k) clearance?

MAX 02 OXYGEN CONCENTRATOR received FDA 510(k) clearance on 1983-11-29, under 510(k) number K833500.

Who is the listed applicant for MAX 02 OXYGEN CONCENTRATOR?

The FDA 510(k) record lists Mountain Medical Equipment, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MAX 02 OXYGEN CONCENTRATOR?

The FDA product code for MAX 02 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 Mountain Medical Equipment, Inc. 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 20 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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