ENDOTRACHEAL TUBE
K-Number: K821243 · 1982-05-21
Advertisement
Device Summary
Frequently Asked Questions
What is the ENDOTRACHEAL TUBE?
ENDOTRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 1982-05-21. The listed applicant is Life-Line Products, Inc.. The 510(k) number is K821243.
When did ENDOTRACHEAL TUBE receive FDA 510(k) clearance?
ENDOTRACHEAL TUBE received FDA 510(k) clearance on 1982-05-21, under 510(k) number K821243.
Who is the listed applicant for ENDOTRACHEAL TUBE?
The FDA 510(k) record lists Life-Line Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOTRACHEAL TUBE?
The FDA product code for ENDOTRACHEAL TUBE is BTR.
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 Life-Line Products, 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: BTR)
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.
Advertisement