Cereve Sleep System— 510(k) DEN140032

Unknown

Cereve, Inc.

FDA 510(k) clearance DEN140032 for Cereve Sleep System, Unknown on 2016-05-13. Applicant: Cereve, Inc.. Device class: 2.

Clearance details

Applicant
Cereve, Inc.
Product code
Code PLU
Device class
Class 2
Regulation
21 CFR 882.5700
Advisory panel
Neurology
Date received
Decision date
Decision
Unknown
Clearance type
Direct
Location
Oakmont, PA, US
View on FDA.gov ↗

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