SNOAR(TM) OPEN AIRWAY APPLIANCE— 510(k) K880956

Name: FDA 510(k) clearance K880956
Creator: U.S. Food and Drug Administration
Published: 1988-05-11

Substantially Equivalent

Kent J. Toone, D.D.S.

FDA 510(k) clearance K880956 for SNOAR(TM) OPEN AIRWAY APPLIANCE, Substantially Equivalent on 1988-05-11. Applicant: Kent J. Toone, D.D.S.. Device class: 2.

Clearance details

Applicant: Kent J. Toone, D.D.S.
Product code: Code LQZ
Device class: Class 2
Regulation: 21 CFR 872.5570
Advisory panel: Dental
Date received: 1988-03-07
Decision date: 1988-05-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cupertino, CA, US

Download summary PDF View on FDA.gov ↗

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