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FDA 510(k)

NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900

K-Number: K032301 · 2003-08-21

ApplicantNeogen Technologies, Inc.
Decision Date2003-08-21
Product CodeOMP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900 is the device name listed in this FDA 510(k) record. The listed applicant is Neogen Technologies, Inc.. It received FDA 510(k) clearance on 2003-08-21 under 510(k) number K032301. The device is classified under product code OMP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900?

NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900 is a medical device that received FDA 510(k) clearance on 2003-08-21. The listed applicant is Neogen Technologies, Inc.. The 510(k) number is K032301.

When did NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900 receive FDA 510(k) clearance?

NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900 received FDA 510(k) clearance on 2003-08-21, under 510(k) number K032301.

Who is the listed applicant for NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900?

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

What is the FDA product code for NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900?

The FDA product code for NEOGEN ONE, CLOSED WOUND DRAIN SYSTEM, PART NUMBER: NG9900 is OMP.

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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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