SEEKER System— 510(k) DEN150035

Unknown

Baebies, Inc.

FDA 510(k) clearance DEN150035 for SEEKER System, Unknown on 2017-02-03. Applicant: Baebies, Inc.. Device class: 2.

Clearance details

Applicant: Baebies, Inc.
Product code: Code PQW
Device class: Class 2
Regulation: 21 CFR 862.1488
Advisory panel: Clinical Chemistry
Date received: 2015-08-05
Decision date: 2017-02-03
Decision: Unknown
Clearance type: Direct
Location: Durham, NC, US

View on FDA.gov ↗

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