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FDA 510(k)

Z TECH TRANSCUTANEOUS NEURAL STIMULATION

K-Number: K965244 · 1997-08-27

Decision Date1997-08-27
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Z TECH TRANSCUTANEOUS NEURAL STIMULATION is the device name listed in this FDA 510(k) record. The listed applicant is Z Technologies, LLC. It received FDA 510(k) clearance on 1997-08-27 under 510(k) number K965244. 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 Z TECH TRANSCUTANEOUS NEURAL STIMULATION?

Z TECH TRANSCUTANEOUS NEURAL STIMULATION is a medical device that received FDA 510(k) clearance on 1997-08-27. The listed applicant is Z Technologies, LLC. The 510(k) number is K965244.

When did Z TECH TRANSCUTANEOUS NEURAL STIMULATION receive FDA 510(k) clearance?

Z TECH TRANSCUTANEOUS NEURAL STIMULATION received FDA 510(k) clearance on 1997-08-27, under 510(k) number K965244.

Who is the listed applicant for Z TECH TRANSCUTANEOUS NEURAL STIMULATION?

The FDA 510(k) record lists Z Technologies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Z TECH TRANSCUTANEOUS NEURAL STIMULATION?

The FDA product code for Z TECH TRANSCUTANEOUS NEURAL STIMULATION 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.

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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