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FDA 510(k)

GROUND/REFERENCE NEEDLE ELECTRODE

K-Number: K933793 · 1994-04-19

ApplicantCadwell Laboratories, Inc.
Decision Date1994-04-19
Product CodeGXZ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

GROUND/REFERENCE NEEDLE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Cadwell Laboratories, Inc.. It received FDA 510(k) clearance on 1994-04-19 under 510(k) number K933793. The device is classified under product code GXZ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GROUND/REFERENCE NEEDLE ELECTRODE?

GROUND/REFERENCE NEEDLE ELECTRODE is a medical device that received FDA 510(k) clearance on 1994-04-19. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K933793.

When did GROUND/REFERENCE NEEDLE ELECTRODE receive FDA 510(k) clearance?

GROUND/REFERENCE NEEDLE ELECTRODE received FDA 510(k) clearance on 1994-04-19, under 510(k) number K933793.

Who is the listed applicant for GROUND/REFERENCE NEEDLE ELECTRODE?

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

What is the FDA product code for GROUND/REFERENCE NEEDLE ELECTRODE?

The FDA product code for GROUND/REFERENCE NEEDLE ELECTRODE is GXZ.

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Other records listing Cadwell Laboratories, Inc. as applicant

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Related Devices (Code: GXZ)

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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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