NASOPHARYNGEAL AIRWAY

Airway, Nasopharyngeal

VESTA, INC.

The following data is part of a premarket notification filed by Vesta, Inc. with the FDA for Nasopharyngeal Airway.

Pre-market Notification Details

Device IDK810960
510k NumberK810960
Device Name:NASOPHARYNGEAL AIRWAY
ClassificationAirway, Nasopharyngeal
Applicant VESTA, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeBTQ  
CFR Regulation Number868.5100 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-04-08
Decision Date1981-04-23

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.