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FDA 510(k)

LIFEBRIDGE

K-Number: K111384 · 2011-05-24

ApplicantLifebridge Medizintechnik AG
Decision Date2011-05-24
Product CodeKFM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LIFEBRIDGE is the device name listed in this FDA 510(k) record. The listed applicant is Lifebridge Medizintechnik AG. It received FDA 510(k) clearance on 2011-05-24 under 510(k) number K111384. 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 LIFEBRIDGE?

LIFEBRIDGE is a medical device that received FDA 510(k) clearance on 2011-05-24. The listed applicant is Lifebridge Medizintechnik AG. The 510(k) number is K111384.

When did LIFEBRIDGE receive FDA 510(k) clearance?

LIFEBRIDGE received FDA 510(k) clearance on 2011-05-24, under 510(k) number K111384.

Who is the listed applicant for LIFEBRIDGE?

The FDA 510(k) record lists Lifebridge Medizintechnik AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LIFEBRIDGE?

The FDA product code for LIFEBRIDGE 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Lifebridge Medizintechnik AG 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.

K103357LIFEBRIDGEK090006LIFEBRIDGE B2T, MODEL 7001

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.

K251762Quantum Perfusion Centrifugal Blood Pump CP20NG with Integrated Sensors (CP20V-NG)Spectrum Medical S.R.L.K250326Quantum Perfusion Centrifugal Blood Pump CP22NG with Integrated Sensors (CP22V-NG)Spectrum Medical S.R.L.K233091Quantum Perfusion Centrifugal Blood Pump CP37 with Integrated Sensors (CP37V-VT); Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors (CP22V-VT)Qura S.R.LK232132LifeSPARC SystemCardiacassist, Inc.K220842Quantum Perfusion Centrifugal Blood Pump CP22 with Integrated Sensors, Quantum Perfusion Centrifugal Blood Pump CP20 with Integrated SensorsQura S.R.LK200091Capiox iCP Centrifugal PumpTerumo Cardiovascular Systems Corporation

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.

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