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FDA 510(k)

Perifix FX Catheter; Contiplex FX Catheter

K-Number: K231242 · 2023-09-15

ApplicantB.Braun Medical, Inc.
Decision Date2023-09-15
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

Perifix FX Catheter; Contiplex FX Catheter is a medical device manufactured by B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2023-09-15 under approval number K231242. The device is classified under product code BSO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Perifix FX Catheter; Contiplex FX Catheter?

Perifix FX Catheter; Contiplex FX Catheter is a medical device that received FDA 510(k) clearance on 2023-09-15. It is manufactured by B.Braun Medical, Inc.. The 510(k) number is K231242.

When was Perifix FX Catheter; Contiplex FX Catheter approved by the FDA?

Perifix FX Catheter; Contiplex FX Catheter received FDA 510(k) clearance on 2023-09-15, under approval number K231242.

What company makes Perifix FX Catheter; Contiplex FX Catheter?

Perifix FX Catheter; Contiplex FX Catheter is manufactured by B.Braun Medical, Inc..

What is the FDA product code for Perifix FX Catheter; Contiplex FX Catheter?

The FDA product code for Perifix FX Catheter; Contiplex FX Catheter is BSO.

Other Devices by B.Braun Medical, Inc.

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Related Devices (Code: BSO)

K161232ON-Q* EchoSpark Echogenic Catheter; ON-Q* T-bloc* Echogenic Continuous Nerve Block KitHalyard Health K153297Perifix and Contiplex CatheterB.Braun Medical, Inc. K152952E-CathPAJUNK GmbH Medizintechnologie K150731Medline Epidural CatheterMedline Industries, Inc. K150789SPINAUT-E, SPINAUT-IImedicom Co., Ltd. K171584B. Braun Tear-Away Introducer NeedleB.Braun Medical, Inc.

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.

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