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FDA 510(k)

C-CAT Anaesthesia Catheter kit

K-Number: K191470 · 2019-10-25

ApplicantCimpax Aps
Decision Date2019-10-25
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

C-CAT Anaesthesia Catheter kit is the device name listed in this FDA 510(k) record. The listed applicant is Cimpax Aps. It received FDA 510(k) clearance on 2019-10-25 under 510(k) number K191470. 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 C-CAT Anaesthesia Catheter kit?

C-CAT Anaesthesia Catheter kit is a medical device that received FDA 510(k) clearance on 2019-10-25. The listed applicant is Cimpax Aps. The 510(k) number is K191470.

When did C-CAT Anaesthesia Catheter kit receive FDA 510(k) clearance?

C-CAT Anaesthesia Catheter kit received FDA 510(k) clearance on 2019-10-25, under 510(k) number K191470.

Who is the listed applicant for C-CAT Anaesthesia Catheter kit?

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

What is the FDA product code for C-CAT Anaesthesia Catheter kit?

The FDA product code for C-CAT Anaesthesia Catheter kit is BSO.

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.K231242Perifix FX Catheter; Contiplex FX CatheterB.Braun Medical, Inc.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.K181782Medline 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.

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