TRACHEOSTOMY T-TUBE
K-Number: K930114 · 1993-03-19
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Device Summary
Frequently Asked Questions
What is the TRACHEOSTOMY T-TUBE?
TRACHEOSTOMY T-TUBE is a medical device that received FDA 510(k) clearance on 1993-03-19. The listed applicant is Invotec International, Inc.. The 510(k) number is K930114.
When did TRACHEOSTOMY T-TUBE receive FDA 510(k) clearance?
TRACHEOSTOMY T-TUBE received FDA 510(k) clearance on 1993-03-19, under 510(k) number K930114.
Who is the listed applicant for TRACHEOSTOMY T-TUBE?
The FDA 510(k) record lists Invotec International, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRACHEOSTOMY T-TUBE?
The FDA product code for TRACHEOSTOMY T-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 Invotec International, 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.
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