Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

PORTABLE OXYGEN GENERATOR

K-Number: K812282 · 1981-10-23

Decision Date1981-10-23
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PORTABLE OXYGEN GENERATOR is the device name listed in this FDA 510(k) record. The listed applicant is American Marketing Assoc., Inc.. It received FDA 510(k) clearance on 1981-10-23 under 510(k) number K812282. 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 PORTABLE OXYGEN GENERATOR?

PORTABLE OXYGEN GENERATOR is a medical device that received FDA 510(k) clearance on 1981-10-23. The listed applicant is American Marketing Assoc., Inc.. The 510(k) number is K812282.

When did PORTABLE OXYGEN GENERATOR receive FDA 510(k) clearance?

PORTABLE OXYGEN GENERATOR received FDA 510(k) clearance on 1981-10-23, under 510(k) number K812282.

Who is the listed applicant for PORTABLE OXYGEN GENERATOR?

The FDA 510(k) record lists American Marketing Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PORTABLE OXYGEN GENERATOR?

The FDA product code for PORTABLE OXYGEN GENERATOR 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.

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.

↑