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FDA 510(k)

SORIN CENTRIFUGAL PUMP 5 (CP5)

K-Number: K112225 · 2011-09-20

ApplicantSorin Group Deutschland GmbH
Decision Date2011-09-20
Product CodeDWA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SORIN CENTRIFUGAL PUMP 5 (CP5) is the device name listed in this FDA 510(k) record. The listed applicant is Sorin Group Deutschland GmbH. It received FDA 510(k) clearance on 2011-09-20 under 510(k) number K112225. The device is classified under product code DWA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SORIN CENTRIFUGAL PUMP 5 (CP5)?

SORIN CENTRIFUGAL PUMP 5 (CP5) is a medical device that received FDA 510(k) clearance on 2011-09-20. The listed applicant is Sorin Group Deutschland GmbH. The 510(k) number is K112225.

When did SORIN CENTRIFUGAL PUMP 5 (CP5) receive FDA 510(k) clearance?

SORIN CENTRIFUGAL PUMP 5 (CP5) received FDA 510(k) clearance on 2011-09-20, under 510(k) number K112225.

Who is the listed applicant for SORIN CENTRIFUGAL PUMP 5 (CP5)?

The FDA 510(k) record lists Sorin Group Deutschland GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SORIN CENTRIFUGAL PUMP 5 (CP5)?

The FDA product code for SORIN CENTRIFUGAL PUMP 5 (CP5) is DWA.

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Other records listing Sorin Group Deutschland GmbH as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K170460Sorin ConnectK131816SORIN CONNECT DATA MANAGEMENT SYSTEMK103468STOCKERT CENTRIFUGAL PUMP (SCP PLUS) (COMPLETE) OR (FOR S5/C5 SYSTEMS)K103762SORIN C5 SYSTEM; 85/C5 MAST ROLLER PUMP SYSTEM 150(1X RP 150 AND CONTROL PANEL WITH CONNECTING CABLES); S5/C5 MAST ROLLEK103469STOCKERT AIR PURGE CONTROL SYSTEM MODEL 23-45-05K103168B-CARE5 (B-CARE5 SENSOR MODULE, VENOUS SENSOR, HOLDER FOR MEASURING HEAD)

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Related Devices (Code: DWA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K232788INSPIRA ART100Inspira Technologies Oxy B.H.N. , Ltd.K230698Anivia SG1000 Pump ConsoleApmtd, Inc.K221491Anivia SG1000 Pump ConsoleApmtd, Inc.K192838Quantumn Centrifugal Drive- High Pressure, Quantum Centrifugal Drive- Medium PressureSpectrum Medical , Ltd.K200306CentriMag Circulatory Support System, CentriMag Return (Arterial) Cannula Kit, CentriMag Drainage (Venous) Cannula KitAbbott (Formerly Thoratec Corporation)K191557CentriMag Acute Circulatory Support SystemThoratec Corporation (Now Part of Abbott)

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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