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FDA 510(k)

MARK III OXYGEN WALKER SYSTEM

K-Number: K820836 · 1982-04-15

Decision Date1982-04-15
Product CodeBYJ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MARK III OXYGEN WALKER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Union Carbide Corp.. It received FDA 510(k) clearance on 1982-04-15 under 510(k) number K820836. The device is classified under product code BYJ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARK III OXYGEN WALKER SYSTEM?

MARK III OXYGEN WALKER SYSTEM is a medical device that received FDA 510(k) clearance on 1982-04-15. The listed applicant is Union Carbide Corp.. The 510(k) number is K820836.

When did MARK III OXYGEN WALKER SYSTEM receive FDA 510(k) clearance?

MARK III OXYGEN WALKER SYSTEM received FDA 510(k) clearance on 1982-04-15, under 510(k) number K820836.

Who is the listed applicant for MARK III OXYGEN WALKER SYSTEM?

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

What is the FDA product code for MARK III OXYGEN WALKER SYSTEM?

The FDA product code for MARK III OXYGEN WALKER SYSTEM is BYJ.

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 Union Carbide 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 69 devices →

Related Devices (Code: BYJ)

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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