OXYGEN SUPPLY TUBING
K-Number: K802071 · 1980-09-16
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Device Summary
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
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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