STERILE AIRWAY

Airway, Oropharyngeal, Anesthesiology

MEDSPEC CORP.

The following data is part of a premarket notification filed by Medspec Corp. with the FDA for Sterile Airway.

Pre-market Notification Details

Device IDK810069
510k NumberK810069
Device Name:STERILE AIRWAY
ClassificationAirway, Oropharyngeal, Anesthesiology
Applicant MEDSPEC CORP. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeCAE  
CFR Regulation Number868.5110 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1981-01-13
Decision Date1981-02-02

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