FDA 510(k)

BD Cathena Safety IV Catheter

K-번호: K201717 · 2020-09-22

신청자Becton Dickinson Infusion Therapy Systems, Inc.

결정일2020-09-22

제품 코드FOZ

자문 위원회HO

결정Substantially Equivalent

기기 요약

BD Cathena Safety IV Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. It received FDA 510(k) clearance on 2020-09-22 under 510(k) number K201717. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

자주 묻는 질문

What is the BD Cathena Safety IV Catheter?

BD Cathena Safety IV Catheter is a medical device that received FDA 510(k) clearance on 2020-09-22. The listed applicant is Becton Dickinson Infusion Therapy Systems, Inc.. The 510(k) number is K201717.

When did BD Cathena Safety IV Catheter receive FDA 510(k) clearance?

BD Cathena Safety IV Catheter received FDA 510(k) clearance on 2020-09-22, under 510(k) number K201717.

Who is the listed applicant for BD Cathena Safety IV Catheter?

The FDA 510(k) record lists Becton Dickinson Infusion Therapy Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BD Cathena Safety IV Catheter?

The FDA product code for BD Cathena Safety IV Catheter is FOZ.

Becton Dickinson Infusion Therapy Systems, Inc.를 신청인으로 등재한 기타 기록

K252137BD Insyte™ IV Catheter K251422BD Saf-T-Intima™ Subcutaneous Catheter System K243403BD Nexiva™ Closed IV Catheter System K251155BD Cathena™ Safety IV Catheter K251654BD Insyte™ Autoguard™ Shielded IV Catheter, BD Insyte™ Autoguard™ BC Shielded IV Catheter and BD Insyte™ Autoguard™ BC Pro Shielded IV Catheter K250682BD Nexiva™ Diffusics™ Closed IV Catheter System and BD Nexiva™ Diffusics™ Closed IV Catheter System with BD MaxZero™ Needle-free Connector

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