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FDA 510(k)

Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG)

K-Number: K251762 · 2025-08-04

Decision Date2025-08-04
Product CodeKFM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG) is the device name listed in this FDA 510(k) record. The listed applicant is Spectrum Medical S.R.L.. It received FDA 510(k) clearance on 2025-08-04 under 510(k) number K251762. The device is classified under product code KFM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG)?

Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG) is a medical device that received FDA 510(k) clearance on 2025-08-04. The listed applicant is Spectrum Medical S.R.L.. The 510(k) number is K251762.

When did Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG) receive FDA 510(k) clearance?

Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG) received FDA 510(k) clearance on 2025-08-04, under 510(k) number K251762.

Who is the listed applicant for Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG)?

The FDA 510(k) record lists Spectrum Medical S.R.L. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG)?

The FDA product code for Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG) is KFM.

Related Clinical Trials

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.

Other records listing Spectrum Medical S.R.L. 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.

Related Devices (Code: KFM)

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.

Official Source

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