SOMNOSCREEN— 510(k) K060708

Substantially Equivalent

Somnomedics GmbH & Co. KG

FDA 510(k) clearance K060708 for SOMNOSCREEN, Substantially Equivalent on 2007-01-24. Applicant: Somnomedics GmbH & Co. KG.

Clearance details

Applicant: Somnomedics GmbH & Co. KG
Product code: Code MNR
Advisory panel: Anesthesiology
Date received: 2006-03-16
Decision date: 2007-01-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Washington, DC, US

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