SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM— 510(k) K080321

Name: FDA 510(k) clearance K080321
Creator: U.S. Food and Drug Administration
Published: 2008-05-23

Substantially Equivalent

Snap Laboratories, LLC

FDA 510(k) clearance K080321 for SNAP MODEL 7 SNORING AND APNEA RECORDING AND ANALYSIS SYSTEM, Substantially Equivalent on 2008-05-23. Applicant: Snap Laboratories, LLC. Device class: 2.

Clearance details

Applicant: Snap Laboratories, LLC
Product code: Code MNR
Device class: Class 2
Regulation: 21 CFR 868.2375
Advisory panel: Anesthesiology
Date received: 2008-02-06
Decision date: 2008-05-23
Decision: Substantially Equivalent
Clearance type: Special
Location: Wheeling, IL, 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.