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FDA 510(k)

MICRO TARGETING ELECTRODE

K-Number: K033173 · 2004-03-24

ApplicantFHC, Inc.
Decision Date2004-03-24
Product CodeGZL
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MICRO TARGETING ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is FHC, Inc.. It received FDA 510(k) clearance on 2004-03-24 under 510(k) number K033173. The device is classified under product code GZL. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO TARGETING ELECTRODE?

MICRO TARGETING ELECTRODE is a medical device that received FDA 510(k) clearance on 2004-03-24. The listed applicant is FHC, Inc.. The 510(k) number is K033173.

When did MICRO TARGETING ELECTRODE receive FDA 510(k) clearance?

MICRO TARGETING ELECTRODE received FDA 510(k) clearance on 2004-03-24, under 510(k) number K033173.

Who is the listed applicant for MICRO TARGETING ELECTRODE?

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

What is the FDA product code for MICRO TARGETING ELECTRODE?

The FDA product code for MICRO TARGETING ELECTRODE is GZL.

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Related Devices (Code: GZL)

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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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