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FDA 510(k)

EZ GRIP DISPOSABLE ELECTRODES

K-Number: K932854 · 1994-02-22

ApplicantAdvanced Adhesives
Decision Date1994-02-22
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EZ GRIP DISPOSABLE 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 1994-02-22 under 510(k) number K932854. 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 DISPOSABLE ELECTRODES?

EZ GRIP DISPOSABLE ELECTRODES is a medical device that received FDA 510(k) clearance on 1994-02-22. The listed applicant is Advanced Adhesives. The 510(k) number is K932854.

When did EZ GRIP DISPOSABLE ELECTRODES receive FDA 510(k) clearance?

EZ GRIP DISPOSABLE ELECTRODES received FDA 510(k) clearance on 1994-02-22, under 510(k) number K932854.

Who is the listed applicant for EZ GRIP DISPOSABLE 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 DISPOSABLE ELECTRODES?

The FDA product code for EZ GRIP DISPOSABLE 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.

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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.

K931108EZ GRIP REUSABLE TENS/NMES ELECTRODES

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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