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FDA 510(k)

STIMULUS - DISSECTION INSTRUMENTS

K-Number: K014165 · 2002-01-22

ApplicantMedtronic Xomed, Inc.
Decision Date2002-01-22
Product CodeETN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

STIMULUS - DISSECTION INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Xomed, Inc.. It received FDA 510(k) clearance on 2002-01-22 under 510(k) number K014165. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STIMULUS - DISSECTION INSTRUMENTS?

STIMULUS - DISSECTION INSTRUMENTS is a medical device that received FDA 510(k) clearance on 2002-01-22. The listed applicant is Medtronic Xomed, Inc.. The 510(k) number is K014165.

When did STIMULUS - DISSECTION INSTRUMENTS receive FDA 510(k) clearance?

STIMULUS - DISSECTION INSTRUMENTS received FDA 510(k) clearance on 2002-01-22, under 510(k) number K014165.

Who is the listed applicant for STIMULUS - DISSECTION INSTRUMENTS?

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

What is the FDA product code for STIMULUS - DISSECTION INSTRUMENTS?

The FDA product code for STIMULUS - DISSECTION INSTRUMENTS is ETN.

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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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