TANTONE MULTI-DAY #633 TENS ELECTRODE
K-Number: K871222 · 1987-05-29
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Device Summary
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
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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