CENTRAL VENOUS PRESSURE SYSTEM - MESPERE VENUS 1000— 510(k) K131085

Name: FDA 510(k) clearance K131085
Creator: U.S. Food and Drug Administration
Published: 2013-08-22

Substantially Equivalent

Mespere Lifesciences, Inc.

FDA 510(k) clearance K131085 for CENTRAL VENOUS PRESSURE SYSTEM - MESPERE VENUS 1000, Substantially Equivalent on 2013-08-22. Applicant: Mespere Lifesciences, Inc.. Device class: 2.

Clearance details

Applicant: Mespere Lifesciences, Inc.
Product code: Code PFA
Device class: Class 2
Regulation: 21 CFR 870.1140
Advisory panel: Cardiovascular
Date received: 2013-04-18
Decision date: 2013-08-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Waterloo, On, CA

Download summary PDF View on FDA.gov ↗

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