LUMENVU CATHETER GUIDANCE SYSTEM— 510(k) K093510

Substantially Equivalent

Sonosite,Inc.

FDA 510(k) clearance K093510 for LUMENVU CATHETER GUIDANCE SYSTEM, Substantially Equivalent on 2010-08-23. Applicant: Sonosite,Inc.. Device class: 2.

Clearance details

Applicant: Sonosite,Inc.
Product code: Code OMF
Device class: Class 2
Regulation: 21 CFR 880.5970
Advisory panel: General Hospital
Date received: 2009-11-12
Decision date: 2010-08-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Philedelphia, PA, 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.