510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K902193Substantially Equivalent

Kevtek Laser-Stop Endotracheal Tube Laser-Stop

Kevtek Medical Products, Inc., Houston TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K902193 is the FDA 510(k) clearance record for KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP, a class II device, cleared for Kevtek Medical Products, Inc. on under FDA product code BTR (Tube, Tracheal (W/Wo Connector)). FDA records list 2 510(k) clearances for Kevtek Medical Products, Inc., from to . As of , FDA records show no recalls naming K902193.

Clearance record

Decision date
Received
(303 days to decision)
Product code
BTR Tube, Tracheal (W/Wo Connector)
Regulation
21 CFR 868.5730
Device class
Class II
Review panel
Anesthesiology
Applicant
Kevtek Medical Products, Inc. P.O. Box 580644, Houston TX
Third party review
No

Clearances, product code BTR

Trailing 12 months
2 clearances under product code BTR in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code BTR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260