Endotracheal Tube Guide or Intubation Stylette

No FDA recalls found in the data synced 22 Oct 2026.

510(k) Number

K854632 ↗

FDA Product Code

BTR

Device Class

Class II

Regulation

21 CFR Part 868.5730

Advisory Committee

Anesthesiology

FDA Decision

SESE Substantially Equivalent

• Bi-Temp Temperature Monitor, Model TM-300D

  Class II

  FDA 510(k) K913082 Active Cleared 11 Dec 1991

• Esophageal Stethoscope W/Thermocouple Type T

  Class II

  FDA 510(k) K864043 Active Cleared 15 Dec 1986

• Bi-Temp Temperature Monitor, Model Tm-400D

  Class II

  FDA 510(k) K912280 Active Cleared 17 Oct 1991

• Adap-Temp Temperature Sensor Adapter

  Class II

  FDA 510(k) K921190 Active Cleared 9 Mar 1993

• Myocardinal Temperature Sensor with Type 400 Serie

  Class II

  FDA 510(k) K920469 Active Cleared 11 Sep 1992

• Cloud 1 Humidification System

  Class II

  FDA 510(k) K983862 Active Cleared 24 May 1999

See all devices from Respiratory Support Products, Inc. →