NDYAG LASER TRACHEAL TUBE
K-Number: K880960 · 1988-04-29
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Device Summary
Frequently Asked Questions
What is the NDYAG LASER TRACHEAL TUBE?
NDYAG LASER TRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 1988-04-29. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K880960.
When did NDYAG LASER TRACHEAL TUBE receive FDA 510(k) clearance?
NDYAG LASER TRACHEAL TUBE received FDA 510(k) clearance on 1988-04-29, under 510(k) number K880960.
Who is the listed applicant for NDYAG LASER 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 NDYAG LASER TRACHEAL TUBE?
The FDA product code for NDYAG LASER 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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