TRACHEAL TUBE FIXATION DEVICE
K-Number: K930179 · 1993-03-03
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Device Summary
Frequently Asked Questions
What is the TRACHEAL TUBE FIXATION DEVICE?
TRACHEAL TUBE FIXATION DEVICE is a medical device that received FDA 510(k) clearance on 1993-03-03. The listed applicant is Garrett Medical Products. The 510(k) number is K930179.
When did TRACHEAL TUBE FIXATION DEVICE receive FDA 510(k) clearance?
TRACHEAL TUBE FIXATION DEVICE received FDA 510(k) clearance on 1993-03-03, under 510(k) number K930179.
Who is the listed applicant for TRACHEAL TUBE FIXATION DEVICE?
The FDA 510(k) record lists Garrett Medical Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TRACHEAL TUBE FIXATION DEVICE?
The FDA product code for TRACHEAL TUBE FIXATION DEVICE 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 Garrett Medical Products 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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