ENDOTRACHEAL TUBE HOLDER
K-Number: K802601 · 1980-12-18
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Device Summary
Frequently Asked Questions
What is the ENDOTRACHEAL TUBE HOLDER?
ENDOTRACHEAL TUBE HOLDER is a medical device that received FDA 510(k) clearance on 1980-12-18. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K802601.
When did ENDOTRACHEAL TUBE HOLDER receive FDA 510(k) clearance?
ENDOTRACHEAL TUBE HOLDER received FDA 510(k) clearance on 1980-12-18, under 510(k) number K802601.
Who is the listed applicant for ENDOTRACHEAL TUBE HOLDER?
The FDA 510(k) record lists Hudson Oxygen Therapy Sales Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOTRACHEAL TUBE HOLDER?
The FDA product code for ENDOTRACHEAL TUBE HOLDER is CBH.
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 Hudson Oxygen Therapy Sales Co. 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: CBH)
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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