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FDA 510(k)

EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM

K-Number: K023233 · 2002-12-13

ApplicantEbi, L.P.
Decision Date2002-12-13
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ebi, L.P.. It received FDA 510(k) clearance on 2002-12-13 under 510(k) number K023233. 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 EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM?

EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM is a medical device that received FDA 510(k) clearance on 2002-12-13. The listed applicant is Ebi, L.P.. The 510(k) number is K023233.

When did EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM receive FDA 510(k) clearance?

EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM received FDA 510(k) clearance on 2002-12-13, under 510(k) number K023233.

Who is the listed applicant for EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM?

The FDA 510(k) record lists Ebi, L.P. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM?

The FDA product code for EBI TARGETCATH FLUORO-GUIDED STEERABLE CATHETER SYSTEM is BSO.

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Other records listing Ebi, L.P. as applicant

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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.K191470C-CAT Anaesthesia Catheter kitCimpax Aps

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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