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FDA 510(k)

LECTEC STIMULATING ELECTRODE

K-Number: K872250 · 1987-08-07

ApplicantLectec Corp.
Decision Date1987-08-07
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

LECTEC STIMULATING ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Lectec Corp.. It received FDA 510(k) clearance on 1987-08-07 under 510(k) number K872250. 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 LECTEC STIMULATING ELECTRODE?

LECTEC STIMULATING ELECTRODE is a medical device that received FDA 510(k) clearance on 1987-08-07. The listed applicant is Lectec Corp.. The 510(k) number is K872250.

When did LECTEC STIMULATING ELECTRODE receive FDA 510(k) clearance?

LECTEC STIMULATING ELECTRODE received FDA 510(k) clearance on 1987-08-07, under 510(k) number K872250.

Who is the listed applicant for LECTEC STIMULATING ELECTRODE?

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

What is the FDA product code for LECTEC STIMULATING ELECTRODE?

The FDA product code for LECTEC STIMULATING ELECTRODE is GXY.

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Other records listing Lectec Corp. as applicant

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Related Devices (Code: GXY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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