PULSION PULSIOCATH PICCO MONITORING KIT, INJECTATE SENSOR TEMPERATURE HOUSING PV 4046— 510(k) K020587

Name: FDA 510(k) clearance K020587
Creator: U.S. Food and Drug Administration
Published: 2002-05-23

Substantially Equivalent

Pulsion Medical Systems AG

FDA 510(k) clearance K020587 for PULSION PULSIOCATH PICCO MONITORING KIT, INJECTATE SENSOR TEMPERATURE HOUSING PV 4046, Substantially Equivalent on 2002-05-23. Applicant: Pulsion Medical Systems AG. Device class: 2.

Clearance details

Applicant: Pulsion Medical Systems AG
Product code: Code KRB
Device class: Class 2
Regulation: 21 CFR 870.1915
Advisory panel: Cardiovascular
Date received: 2002-02-22
Decision date: 2002-05-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Concord, MA, US

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