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FDA 510(k)

UltraCath Continuous Nerve block Catheter

K-Number: K162522 · 2017-03-17

ApplicantTeleflexmedical, Inc.
Decision Date2017-03-17
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UltraCath Continuous Nerve block Catheter is the device name listed in this FDA 510(k) record. The listed applicant is Teleflexmedical, Inc.. It received FDA 510(k) clearance on 2017-03-17 under 510(k) number K162522. 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 UltraCath Continuous Nerve block Catheter?

UltraCath Continuous Nerve block Catheter is a medical device that received FDA 510(k) clearance on 2017-03-17. The listed applicant is Teleflexmedical, Inc.. The 510(k) number is K162522.

When did UltraCath Continuous Nerve block Catheter receive FDA 510(k) clearance?

UltraCath Continuous Nerve block Catheter received FDA 510(k) clearance on 2017-03-17, under 510(k) number K162522.

Who is the listed applicant for UltraCath Continuous Nerve block Catheter?

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

What is the FDA product code for UltraCath Continuous Nerve block Catheter?

The FDA product code for UltraCath Continuous Nerve block Catheter is BSO.

Related Clinical Trials

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.

NCT07052721Randomized Study of an Analgesic Device Enabling Local Anesthetic Delivery and Neuromodulation After Shoulder/Foot SurgeryCOMPLETEDNCT07638514Postoperative Analgesia Using a Perineural Catheter Versus a Single Nerve Block in Rearfoot SurgeryNOT_YET_RECRUITINGNCT03747146Enhanced Recovery After Surgery (ERAS) Total Knee Replacement (TKR) With a Transitional Pain ServiceRECRUITING

Other records listing Teleflexmedical, Inc. 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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