DYNASENSE SYSTEM— 510(k) K130752

Substantially Equivalent

Centauri Medical, Inc.

FDA 510(k) clearance K130752 for DYNASENSE SYSTEM, Substantially Equivalent on 2013-08-15. Applicant: Centauri Medical, Inc.. Device class: 1.

Clearance details

Applicant: Centauri Medical, Inc.
Product code: Code KMI
Device class: Class 1
Regulation: 21 CFR 880.2400
Advisory panel: General Hospital
Date received: 2013-03-19
Decision date: 2013-08-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

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