SOMNOSCREEN EEG10-20— 510(k) K071556

Substantially Equivalent

Somnomedics GmbH

FDA 510(k) clearance K071556 for SOMNOSCREEN EEG10-20, Substantially Equivalent on 2007-07-18. Applicant: Somnomedics GmbH. Device class: 2.

Clearance details

Applicant
Somnomedics GmbH
Product code
Code MNR
Device class
Class 2
Regulation
21 CFR 868.2375
Advisory panel
Anesthesiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Special
Location
Washington, DC, US
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