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FDA 510(k)

MICOR CONDUCTION CATHETER

K-Number: K001717 · 2000-09-20

ApplicantMicor, Inc.
Decision Date2000-09-20
Product CodeBSO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MICOR CONDUCTION CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Micor, Inc.. It received FDA 510(k) clearance on 2000-09-20 under 510(k) number K001717. 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 MICOR CONDUCTION CATHETER?

MICOR CONDUCTION CATHETER is a medical device that received FDA 510(k) clearance on 2000-09-20. The listed applicant is Micor, Inc.. The 510(k) number is K001717.

When did MICOR CONDUCTION CATHETER receive FDA 510(k) clearance?

MICOR CONDUCTION CATHETER received FDA 510(k) clearance on 2000-09-20, under 510(k) number K001717.

Who is the listed applicant for MICOR CONDUCTION CATHETER?

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

What is the FDA product code for MICOR CONDUCTION CATHETER?

The FDA product code for MICOR CONDUCTION 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.

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Other records listing Micor, 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.

K031600CONDUCTION CATHETERK003966WUNDCATH CONDUCTION CATHETERK001940MICOR ANESTHESIA CONDUCTION KITK991879SPRING-WOUND EPIDURAL CATHETERK861008PERCUTANEOUS CATHETERSK860339PERCUTANEOUS CATHETERS

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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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