SNOREX— 510(k) K971818

Substantially Equivalent

Snorex (Nz) , Ltd.

FDA 510(k) clearance K971818 for SNOREX, Substantially Equivalent on 1997-12-18. Applicant: Snorex (Nz) , Ltd.. Device class: 2.

Clearance details

Applicant: Snorex (Nz) , Ltd.
Product code: Code LQZ
Device class: Class 2
Regulation: 21 CFR 872.5570
Advisory panel: Dental
Date received: 1997-05-16
Decision date: 1997-12-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Springfield, VA, 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.