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FDA 510(k)

DUAL TYPE ELECTRODE

K-Number: K810206 · 1981-03-20

ApplicantProfessional Instruments Co.
Decision Date1981-03-20
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DUAL TYPE ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Professional Instruments Co.. It received FDA 510(k) clearance on 1981-03-20 under 510(k) number K810206. The device is classified under product code GXY. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL TYPE ELECTRODE?

DUAL TYPE ELECTRODE is a medical device that received FDA 510(k) clearance on 1981-03-20. The listed applicant is Professional Instruments Co.. The 510(k) number is K810206.

When did DUAL TYPE ELECTRODE receive FDA 510(k) clearance?

DUAL TYPE ELECTRODE received FDA 510(k) clearance on 1981-03-20, under 510(k) number K810206.

Who is the listed applicant for DUAL TYPE ELECTRODE?

The FDA 510(k) record lists Professional Instruments Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DUAL TYPE ELECTRODE?

The FDA product code for DUAL TYPE ELECTRODE is GXY.

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Other records listing Professional Instruments Co. as applicant

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Related Devices (Code: GXY)

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Official Source

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