CAPNIA, INC.

FDA Device Registration & Listing · Foster City, CA, US · Registration 3008614998

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3008614998
FEI Number
3008614998
Entity Name
CAPNIA, INC.
City/State/Country
Foster City, CA, US
Establishment Address
1101 Chess Drive, Foster City, CA 94404, US
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Capnia, Inc. (Owner Number: 10042955)
Owner / Operator Contact Address
1101 Chess Drive, Foster City, CA 94404, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K130036
PMA Number
N/A

All Registered Proprietary Names

CoSense CO Monitor CoSense ETCO Monitor CoSense End Tidal Carbon Monoxide Monitor

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
CCJ Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase Anesthesiology Class 2 868.1430 2013-01-14
CCJ Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase Anesthesiology Class 2 868.1430 2015-09-16
CCJ Analyzer, Gas, Carbon-Monoxide, Gaseous-Phase Anesthesiology Class 2 868.1430 2014-12-23

Official Correspondent

Edwin Baumann

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

Capnia, Inc.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3008614998. Last updated year: 2026. Please use registration number 3008614998 when referencing this establishment in official correspondence.
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