Cardiovascular Pressure Measurement (CPM) System, Navvus Catheter

FDA 510(k) K132474 · Acist Medical Systems

Substantially Equivalent

510(k) numberK132474

Submission

Device name
Cardiovascular Pressure Measurement (CPM) System, Navvus Catheter
Applicant
Acist Medical Systems
Eden Prairie, MN, US
Received
August 7, 2013
Decision date
January 30, 2014
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DXO – Transducer, Pressure, Catheter Tip
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2870
Specialty
Cardiovascular

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Questions and answers

When was Cardiovascular Pressure Measurement (CPM) System, Navvus Catheter cleared by the FDA?

Cardiovascular Pressure Measurement (CPM) System, Navvus Catheter (K132474) received a 510(k) decision of Substantially Equivalent on January 30, 2014, 176 days after the submission was received.

What is the product code of K132474?

The FDA product code is DXO – Transducer, Pressure, Catheter Tip, a Class II (moderate risk) device regulated under 21 CFR 870.2870.