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FDA 510(k)

OXYGEN SUPPLY TUBING

K-Number: K802071 · 1980-09-16

Decision Date1980-09-16
Product CodeBYX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYGEN SUPPLY TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Auburn Components. It received FDA 510(k) clearance on 1980-09-16 under 510(k) number K802071. The device is classified under product code BYX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXYGEN SUPPLY TUBING?

OXYGEN SUPPLY TUBING is a medical device that received FDA 510(k) clearance on 1980-09-16. The listed applicant is Auburn Components. The 510(k) number is K802071.

When did OXYGEN SUPPLY TUBING receive FDA 510(k) clearance?

OXYGEN SUPPLY TUBING received FDA 510(k) clearance on 1980-09-16, under 510(k) number K802071.

Who is the listed applicant for OXYGEN SUPPLY TUBING?

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

What is the FDA product code for OXYGEN SUPPLY TUBING?

The FDA product code for OXYGEN SUPPLY TUBING is BYX.

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: BYX)

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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