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FDA 510(k)

VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS

K-Number: K040751 · 2005-03-10

Decision Date2005-03-10
Product CodeNLH
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS is the device name listed in this FDA 510(k) record. The listed applicant is Vanguard Medical Concepts, Inc.. It received FDA 510(k) clearance on 2005-03-10 under 510(k) number K040751. The device is classified under product code NLH. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS?

VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS is a medical device that received FDA 510(k) clearance on 2005-03-10. The listed applicant is Vanguard Medical Concepts, Inc.. The 510(k) number is K040751.

When did VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS receive FDA 510(k) clearance?

VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS received FDA 510(k) clearance on 2005-03-10, under 510(k) number K040751.

Who is the listed applicant for VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS?

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

What is the FDA product code for VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS?

The FDA product code for VANGUARD REPROCESSED DIAGNOSTIC ELECTROPHYSIOLOGY CATHETERS is NLH.

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.

Other records listing Vanguard Medical Concepts, 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.

View all 33 devices →

Related Devices (Code: NLH)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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