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FDA 510(k)

TENS ELECTRODE SNAP TYPE, DISPOSA., SELF-ADHERING

K-Number: K880649 · 1988-03-04

ApplicantLabeltape Meditect, Inc.
Decision Date1988-03-04
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TENS ELECTRODE SNAP TYPE, DISPOSA., SELF-ADHERING is the device name listed in this FDA 510(k) record. The listed applicant is Labeltape Meditect, Inc.. It received FDA 510(k) clearance on 1988-03-04 under 510(k) number K880649. 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 SNAP TYPE, DISPOSA., SELF-ADHERING?

TENS ELECTRODE SNAP TYPE, DISPOSA., SELF-ADHERING is a medical device that received FDA 510(k) clearance on 1988-03-04. The listed applicant is Labeltape Meditect, Inc.. The 510(k) number is K880649.

When did TENS ELECTRODE SNAP TYPE, DISPOSA., SELF-ADHERING receive FDA 510(k) clearance?

TENS ELECTRODE SNAP TYPE, DISPOSA., SELF-ADHERING received FDA 510(k) clearance on 1988-03-04, under 510(k) number K880649.

Who is the listed applicant for TENS ELECTRODE SNAP TYPE, DISPOSA., SELF-ADHERING?

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

What is the FDA product code for TENS ELECTRODE SNAP TYPE, DISPOSA., SELF-ADHERING?

The FDA product code for TENS ELECTRODE SNAP TYPE, DISPOSA., SELF-ADHERING is 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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