FDA 510(k)

RF INTRODUCTION CANNULA

K-Number: K041021 · 2004-09-16

Decision Date2004-09-16

Product CodeGXI

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

RF INTRODUCTION CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Epimed International, Inc.. It received FDA 510(k) clearance on 2004-09-16 under 510(k) number K041021. The device is classified under product code GXI. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RF INTRODUCTION CANNULA?

RF INTRODUCTION CANNULA is a medical device that received FDA 510(k) clearance on 2004-09-16. The listed applicant is Epimed International, Inc.. The 510(k) number is K041021.

When did RF INTRODUCTION CANNULA receive FDA 510(k) clearance?

RF INTRODUCTION CANNULA received FDA 510(k) clearance on 2004-09-16, under 510(k) number K041021.

Who is the listed applicant for RF INTRODUCTION CANNULA?

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

What is the FDA product code for RF INTRODUCTION CANNULA?

The FDA product code for RF INTRODUCTION CANNULA is GXI.

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Related Devices (Code: GXI)

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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.