DeviceClearance

Product code BTP— Anesthesiology

ANAPNOGUARD ENDOTRACHEAL TUBE

Classification name
Dropper, Ether
Device class
Class 1
Regulation
21 CFR 868.5420
Advisory panel
Anesthesiology
Total cleared
1
First cleared
Most recent

Market context for product code BTP

FDA has cleared 1 device under product code BTP, all in 2010, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Top applicants under product code BTP

Recent clearances under product code BTP

Data sourced from openFDA. This site is unofficial and independent of the FDA.