SureSigns VS3, SureSigns VS4— 510(k) K151761

Name: FDA 510(k) clearance K151761
Creator: U.S. Food and Drug Administration
Published: 2015-09-29

Substantially Equivalent

Phillips Medical Systems

FDA 510(k) clearance K151761 for SureSigns VS3, SureSigns VS4, Substantially Equivalent on 2015-09-29. Applicant: Phillips Medical Systems. Device class: 2.

Clearance details

Applicant: Phillips Medical Systems
Product code: Code DSJ
Device class: Class 2
Regulation: 21 CFR 870.1100
Advisory panel: Cardiovascular
Date received: 2015-06-29
Decision date: 2015-09-29
Decision: Substantially Equivalent
Clearance type: Special
Location: Andover, MA, 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.