FDA 510(k)

FloPump 57mL 离心泵

K号: K193663 · 2021-03-10

决定日期2021-03-10

产品代码KFM

咨询委员会CV 请注意，由于原文未提供具体内容，以下是一个示例翻译： --- 产品名称：[产品名称] 公司名称：[公司名称] FDA批准号：[FDA批准号] 510(k)申请号：[510(k)申请号] PMA申请号：[PMA申请号] 临床试验注册号：[NCT] PubMed ID：[PMID] 产品标识符：[标识符] 产品URL：[URL] --- 请将上述示例中的[产品名称]、[公司名称]、[FDA批准号]等占位符替换为实际内容。

决定实质等同

器械摘要

FloPump 57mL Centrifugal Pump is the device name listed in this FDA 510(k) record. The listed applicant is International Biophysics Corporation. It received FDA 510(k) clearance on 2021-03-10 under 510(k) number K193663. The device is classified under product code KFM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

常见问题

What is the FloPump 57mL Centrifugal Pump?

FloPump 57mL Centrifugal Pump is a medical device that received FDA 510(k) clearance on 2021-03-10. The listed applicant is International Biophysics Corporation. The 510(k) number is K193663.

When did FloPump 57mL Centrifugal Pump receive FDA 510(k) clearance?

FloPump 57mL Centrifugal Pump received FDA 510(k) clearance on 2021-03-10, under 510(k) number K193663.

Who is the listed applicant for FloPump 57mL Centrifugal Pump?

The FDA 510(k) record lists International Biophysics Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FloPump 57mL Centrifugal Pump?

The FDA product code for FloPump 57mL Centrifugal Pump is KFM.

列明International Biophysics Corporation为申报人的其他记录

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K170029FloPump 32mL，无菌，FloPump 32mL，非无菌

相关器械（代码：KFM）

关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系；请查阅链接的官方来源。

K251762Quantum 灌注离心血泵 CP20NG 集成传感器（CP20V-NG）Spectrum Medical S.R.L.K250326Quantum 灌注离心血泵 CP22NG 集成传感器（CP22V-NG）Spectrum Medical S.R.L.K233091Quantum 灌注离心血泵 CP37 集成传感器（CP37V-VT）；Quantum 灌注离心血泵 CP22 集成传感器（CP22V-VT）Qura S.R.L K232132LifeSPARC 系统Cardiacassist, Inc.K220842Quantum 灌注离心血泵 CP22 集成传感器，Quantum 灌注离心血泵 CP20 集成传感器Qura S.R.L K200091Capiox iCP 离心泵Terumo Cardiovascular Systems Corporation

官方来源

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