KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP
K-Number: K902193 · 1991-03-15
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Device Summary
Frequently Asked Questions
What is the KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP?
KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP is a medical device that received FDA 510(k) clearance on 1991-03-15. The listed applicant is Kevtek Medical Products, Inc.. The 510(k) number is K902193.
When did KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP receive FDA 510(k) clearance?
KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP received FDA 510(k) clearance on 1991-03-15, under 510(k) number K902193.
Who is the listed applicant for KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP?
The FDA 510(k) record lists Kevtek Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP?
The FDA product code for KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP 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 Kevtek Medical Products, 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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