LAZER-TRACH TRACHEAL TUBE
K-Number: K922894 · 1993-05-07
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Device Summary
Frequently Asked Questions
What is the LAZER-TRACH TRACHEAL TUBE?
LAZER-TRACH TRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 1993-05-07. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K922894.
When did LAZER-TRACH TRACHEAL TUBE receive FDA 510(k) clearance?
LAZER-TRACH TRACHEAL TUBE received FDA 510(k) clearance on 1993-05-07, under 510(k) number K922894.
Who is the listed applicant for LAZER-TRACH 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 LAZER-TRACH TRACHEAL TUBE?
The FDA product code for LAZER-TRACH 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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