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FDA 510(k)

TENS ELECTRODE MODEL 238P

K-Number: K881872 · 1988-06-16

ApplicantLectec Corp.
Decision Date1988-06-16
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TENS ELECTRODE MODEL 238P is the device name listed in this FDA 510(k) record. The listed applicant is Lectec Corp.. It received FDA 510(k) clearance on 1988-06-16 under 510(k) number K881872. 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 TENS ELECTRODE MODEL 238P?

TENS ELECTRODE MODEL 238P is a medical device that received FDA 510(k) clearance on 1988-06-16. The listed applicant is Lectec Corp.. The 510(k) number is K881872.

When did TENS ELECTRODE MODEL 238P receive FDA 510(k) clearance?

TENS ELECTRODE MODEL 238P received FDA 510(k) clearance on 1988-06-16, under 510(k) number K881872.

Who is the listed applicant for TENS ELECTRODE MODEL 238P?

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 TENS ELECTRODE MODEL 238P?

The FDA product code for TENS ELECTRODE MODEL 238P is GXY.

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Related Devices (Code: GXY)

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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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