FDA 510(k)

SPECT.E.N.S. REPOSTION.-E FOAM PIN TYPE TENS ELECT

K-Number: K902719 · 1990-07-19

Decision Date1990-07-19

Product CodeGXY

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

SPECT.E.N.S. REPOSTION.-E FOAM PIN TYPE TENS ELECT 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 1990-07-19 under 510(k) number K902719. 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 SPECT.E.N.S. REPOSTION.-E FOAM PIN TYPE TENS ELECT?

SPECT.E.N.S. REPOSTION.-E FOAM PIN TYPE TENS ELECT is a medical device that received FDA 510(k) clearance on 1990-07-19. The listed applicant is Labeltape Meditect, Inc.. The 510(k) number is K902719.

When did SPECT.E.N.S. REPOSTION.-E FOAM PIN TYPE TENS ELECT receive FDA 510(k) clearance?

SPECT.E.N.S. REPOSTION.-E FOAM PIN TYPE TENS ELECT received FDA 510(k) clearance on 1990-07-19, under 510(k) number K902719.

Who is the listed applicant for SPECT.E.N.S. REPOSTION.-E FOAM PIN TYPE TENS ELECT?

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 SPECT.E.N.S. REPOSTION.-E FOAM PIN TYPE TENS ELECT?

The FDA product code for SPECT.E.N.S. REPOSTION.-E FOAM PIN TYPE TENS ELECT is GXY.

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Other records listing Labeltape Meditect, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.