DeviceClearance

AIRSONNETT AIRSHOWER AIR 3— 510(k) K081062

Substantially Equivalent

Airsonett, Inc.

FDA 510(k) clearance K081062 for AIRSONNETT AIRSHOWER AIR 3, Substantially Equivalent on 2008-11-07. Applicant: Airsonett, Inc.. Device class: 2.

Clearance details

Applicant
Airsonett, Inc.
Product code
Code FRF
Device class
Class 2
Regulation
21 CFR 880.5045
Advisory panel
General Hospital
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Findley, MN, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code FRF

view all

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