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FDA 510(k)

EZ GRIP REUSABLE TENS/NMES ELECTRODES

K-Number: K931108 · 1994-02-01

Decision Date1994-02-01
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EZ GRIP REUSABLE TENS/NMES ELECTRODES is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Adhesives. It received FDA 510(k) clearance on 1994-02-01 under 510(k) number K931108. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EZ GRIP REUSABLE TENS/NMES ELECTRODES?

EZ GRIP REUSABLE TENS/NMES ELECTRODES is a medical device that received FDA 510(k) clearance on 1994-02-01. The listed applicant is Advanced Adhesives. The 510(k) number is K931108.

When did EZ GRIP REUSABLE TENS/NMES ELECTRODES receive FDA 510(k) clearance?

EZ GRIP REUSABLE TENS/NMES ELECTRODES received FDA 510(k) clearance on 1994-02-01, under 510(k) number K931108.

Who is the listed applicant for EZ GRIP REUSABLE TENS/NMES ELECTRODES?

The FDA 510(k) record lists Advanced Adhesives as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EZ GRIP REUSABLE TENS/NMES ELECTRODES?

The FDA product code for EZ GRIP REUSABLE TENS/NMES ELECTRODES is GZJ.

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 Advanced Adhesives 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: GZJ)

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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