FDA 510(k)

REPROCESSED DISPOSABLE CUTTERS, STAPLERS AND APPLIERS

K-Number: K032973 · 2003-12-18

ApplicantVanguard Medical Concepts, Inc.

Decision Date2003-12-18

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

REPROCESSED DISPOSABLE CUTTERS, STAPLERS AND APPLIERS 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 2003-12-18 under 510(k) number K032973. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED DISPOSABLE CUTTERS, STAPLERS AND APPLIERS?

REPROCESSED DISPOSABLE CUTTERS, STAPLERS AND APPLIERS is a medical device that received FDA 510(k) clearance on 2003-12-18. The listed applicant is Vanguard Medical Concepts, Inc.. The 510(k) number is K032973.

When did REPROCESSED DISPOSABLE CUTTERS, STAPLERS AND APPLIERS receive FDA 510(k) clearance?

REPROCESSED DISPOSABLE CUTTERS, STAPLERS AND APPLIERS received FDA 510(k) clearance on 2003-12-18, under 510(k) number K032973.

Who is the listed applicant for REPROCESSED DISPOSABLE CUTTERS, STAPLERS AND APPLIERS?

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 REPROCESSED DISPOSABLE CUTTERS, STAPLERS AND APPLIERS?

The FDA product code for REPROCESSED DISPOSABLE CUTTERS, STAPLERS AND APPLIERS is GDW.

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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.