OXYGEN TUBING (CRUSH RESISTANT)/VINYL TP
K-Number: K801190 · 1980-05-23
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Device Summary
Frequently Asked Questions
What is the OXYGEN TUBING (CRUSH RESISTANT)/VINYL TP?
OXYGEN TUBING (CRUSH RESISTANT)/VINYL TP is a medical device that received FDA 510(k) clearance on 1980-05-23. The listed applicant is Airlife, Inc.. The 510(k) number is K801190.
When did OXYGEN TUBING (CRUSH RESISTANT)/VINYL TP receive FDA 510(k) clearance?
OXYGEN TUBING (CRUSH RESISTANT)/VINYL TP received FDA 510(k) clearance on 1980-05-23, under 510(k) number K801190.
Who is the listed applicant for OXYGEN TUBING (CRUSH RESISTANT)/VINYL TP?
The FDA 510(k) record lists Airlife, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXYGEN TUBING (CRUSH RESISTANT)/VINYL TP?
The FDA product code for OXYGEN TUBING (CRUSH RESISTANT)/VINYL TP 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.
Other records listing Airlife, Inc. 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.
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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