BELL/MCKAY TRACHEAL TUBE
K-Number: K872616 · 1987-08-10
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Device Summary
Frequently Asked Questions
What is the BELL/MCKAY TRACHEAL TUBE?
BELL/MCKAY TRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 1987-08-10. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K872616.
When did BELL/MCKAY TRACHEAL TUBE receive FDA 510(k) clearance?
BELL/MCKAY TRACHEAL TUBE received FDA 510(k) clearance on 1987-08-10, under 510(k) number K872616.
Who is the listed applicant for BELL/MCKAY TRACHEAL TUBE?
The FDA 510(k) record lists Sheridan Catheter Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BELL/MCKAY TRACHEAL TUBE?
The FDA product code for BELL/MCKAY TRACHEAL 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 Sheridan Catheter Corp. 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.
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