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FDA 510(k)

MEDOX OXYGEN SYSTEM

K-Number: K823172 · 1983-02-01

ApplicantMepecc Intl.
Decision Date1983-02-01
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDOX OXYGEN SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mepecc Intl.. It received FDA 510(k) clearance on 1983-02-01 under 510(k) number K823172. 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 MEDOX OXYGEN SYSTEM?

MEDOX OXYGEN SYSTEM is a medical device that received FDA 510(k) clearance on 1983-02-01. The listed applicant is Mepecc Intl.. The 510(k) number is K823172.

When did MEDOX OXYGEN SYSTEM receive FDA 510(k) clearance?

MEDOX OXYGEN SYSTEM received FDA 510(k) clearance on 1983-02-01, under 510(k) number K823172.

Who is the listed applicant for MEDOX OXYGEN SYSTEM?

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

What is the FDA product code for MEDOX OXYGEN SYSTEM?

The FDA product code for MEDOX OXYGEN SYSTEM is CAW.

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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.

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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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