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FDA 510(k)

VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL

K-Number: K043315 · 2005-03-22

ApplicantVanguard Medical Concepts, Inc.
Decision Date2005-03-22
Product CodeNLQ
DecisionSubstantially Equivalent

Device Summary

VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL 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 2005-03-22 under 510(k) number K043315. The device is classified under product code NLQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL?

VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL is a medical device that received FDA 510(k) clearance on 2005-03-22. The listed applicant is Vanguard Medical Concepts, Inc.. The 510(k) number is K043315.

When did VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL receive FDA 510(k) clearance?

VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL received FDA 510(k) clearance on 2005-03-22, under 510(k) number K043315.

Who is the listed applicant for VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL?

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 HAND-ACTIVATED ULTRASONIC SCALPEL?

The FDA product code for VANGUARD REPROCESSED HAND-ACTIVATED ULTRASONIC SCALPEL is NLQ.

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Other records listing Vanguard Medical Concepts, Inc. as applicant

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Related Devices (Code: NLQ)

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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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