Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

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 the device name listed in this FDA 510(k) record. The listed applicant is B.Braun Medical, Inc.. It received FDA 510(k) clearance on 2023-09-15 under 510(k) 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. The listed applicant is B.Braun Medical, Inc.. The 510(k) number is K231242.

When did Perifix FX Catheter; Contiplex FX Catheter receive FDA 510(k) clearance?

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

Who is the listed applicant for Perifix FX Catheter; Contiplex FX Catheter?

The FDA 510(k) record lists B.Braun Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 records listing B.Braun Medical, Inc. 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.

K253235Introcan Safety® Deep Access XL IV CatheterK243392Infusomat® Space Volumetric Infusion Pump Administration SetsK240578VenaTech® LP Vena Cava Filter System and VenaTech® Convertible Vena Cava Filter SystemK241845Introcan Safety® 2 IV CatheterK241385Omnifix Syringe NRFitK223479AQUAbase nX

View all 34 devices →

Related Devices (Code: BSO)

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.

K241410EDEN ControlCathJmt Co., Ltd.K230603Arrow Non-Stimulating SnapLock Adapter (K-05520-005C); Arrow Non-Stimulating Next Gen SnapLock Adapter (Luer Connection) (CA-000010-19); Arrow Non-Stimulating Next Gen SnapLock Adapter (Neuraxial Connection) (CA-000014-19); Arrow Stimulating SnapLock Adapter (with cable) (TZ-02060-001); Arrow Stimulating SnapLock Adapter (with tab) (TZ-05000-002)Teleflex MedicalK193664SubQKath Catheter and Needle SetHk SurgicalK200624Percutaneous IntroducerEpimed International, Inc.K191470C-CAT Anaesthesia Catheter kitCimpax ApsK181782Medline Reinforced Epidural CatheterMedline Industries, 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.

↑