Nipro SafeTouch IV Catheter
K-Number: K161681 · 2017-03-08
ApplicantNipro Medical Corporation
Decision Date2017-03-08
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
Nipro SafeTouch IV Catheter is a medical device manufactured by Nipro Medical Corporation. It received FDA 510(k) clearance on 2017-03-08 under approval number K161681. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Nipro SafeTouch IV Catheter?
Nipro SafeTouch IV Catheter is a medical device that received FDA 510(k) clearance on 2017-03-08. It is manufactured by Nipro Medical Corporation. The 510(k) number is K161681.
When was Nipro SafeTouch IV Catheter approved by the FDA?
Nipro SafeTouch IV Catheter received FDA 510(k) clearance on 2017-03-08, under approval number K161681.
What company makes Nipro SafeTouch IV Catheter?
Nipro SafeTouch IV Catheter is manufactured by Nipro Medical Corporation.
What is the FDA product code for Nipro SafeTouch IV Catheter?
The FDA product code for Nipro SafeTouch IV Catheter is FOZ.
Other Devices by Nipro Medical Corporation
Related Devices (Code: FOZ)
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K162377PowerGlide Pro Midline CatheterC.R. Bard, Inc.
K161866BioFlo Midline CatheterNavilyst Medical, Inc.
K161777BD Nexiva and BD Nexiva Diffusics Closed IV Catheter SystemsBecton Dickinson Infusion Therapy Systems, Inc.
K160592SUPERCATH 6Togo Medikit Co., Ltd.
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.