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FDA 510(k)

THE VANGUARD SYSTEM

K-Number: K941551 · 1995-01-13

ApplicantCleveland Clinic Foundation
Decision Date1995-01-13
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

THE VANGUARD SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Cleveland Clinic Foundation. It received FDA 510(k) clearance on 1995-01-13 under 510(k) number K941551. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE VANGUARD SYSTEM?

THE VANGUARD SYSTEM is a medical device that received FDA 510(k) clearance on 1995-01-13. The listed applicant is Cleveland Clinic Foundation. The 510(k) number is K941551.

When did THE VANGUARD SYSTEM receive FDA 510(k) clearance?

THE VANGUARD SYSTEM received FDA 510(k) clearance on 1995-01-13, under 510(k) number K941551.

Who is the listed applicant for THE VANGUARD SYSTEM?

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

What is the FDA product code for THE VANGUARD SYSTEM?

The FDA product code for THE VANGUARD SYSTEM is GWQ.

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Related Devices (Code: GWQ)

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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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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