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FDA 510(k)

VANGUARD REPROCESSED ARTHROSCOPIC WANDS

K-Number: K043198 · 2005-05-27

ApplicantVanguard Medical Concepts, Inc.
Decision Date2005-05-27
Product CodeNUJ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

VANGUARD REPROCESSED ARTHROSCOPIC WANDS 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 2005-05-27 under 510(k) number K043198. The device is classified under product code NUJ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VANGUARD REPROCESSED ARTHROSCOPIC WANDS?

VANGUARD REPROCESSED ARTHROSCOPIC WANDS is a medical device that received FDA 510(k) clearance on 2005-05-27. The listed applicant is Vanguard Medical Concepts, Inc.. The 510(k) number is K043198.

When did VANGUARD REPROCESSED ARTHROSCOPIC WANDS receive FDA 510(k) clearance?

VANGUARD REPROCESSED ARTHROSCOPIC WANDS received FDA 510(k) clearance on 2005-05-27, under 510(k) number K043198.

Who is the listed applicant for VANGUARD REPROCESSED ARTHROSCOPIC WANDS?

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 ARTHROSCOPIC WANDS?

The FDA product code for VANGUARD REPROCESSED ARTHROSCOPIC WANDS is NUJ.

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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.

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Related Devices (Code: NUJ)

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.

K232511Medline ReNewal Reprocessed LigaSure Exact Dissector, Nano-coated (LF2019)Surgical Instrument Service and Savings, Inc.K230251Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)Stryker Sustainability SolutionsK220411Reprocessed LigaSure Curved, Small Jaw, Open Sealer/Divider (LF1212A)Stryker Sustainability SolutionsK211203Green OR Reprocessed Aquamantys Bipolar SealerGreen Or, LLCK191073Vein360 Endovenous Radiofrequency Ablation (RFA) CatheterVein 360, LLCK182588Medline ReNewal Reprocessed LigaSure Maryland Jaw Sealer/DividerSurgical Instrument Service and Savings Inc.(Dba Medline Ren

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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