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FDA 510(k)

TANTONE MULTI-DAY #633 TENS ELECTRODE

K-Number: K871222 · 1987-05-29

Decision Date1987-05-29
Product CodeGXY
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

TANTONE MULTI-DAY #633 TENS ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Uni-Patch, Inc.. It received FDA 510(k) clearance on 1987-05-29 under 510(k) number K871222. 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 TANTONE MULTI-DAY #633 TENS ELECTRODE?

TANTONE MULTI-DAY #633 TENS ELECTRODE is a medical device that received FDA 510(k) clearance on 1987-05-29. The listed applicant is Uni-Patch, Inc.. The 510(k) number is K871222.

When did TANTONE MULTI-DAY #633 TENS ELECTRODE receive FDA 510(k) clearance?

TANTONE MULTI-DAY #633 TENS ELECTRODE received FDA 510(k) clearance on 1987-05-29, under 510(k) number K871222.

Who is the listed applicant for TANTONE MULTI-DAY #633 TENS ELECTRODE?

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

What is the FDA product code for TANTONE MULTI-DAY #633 TENS ELECTRODE?

The FDA product code for TANTONE MULTI-DAY #633 TENS ELECTRODE is GXY.

Related Clinical Trials

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.

Other records listing Uni-Patch, Inc. as applicant

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.

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.

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.

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