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FDA 510(k)

SHE-LI TENS STIMULATOR MODEL SL-101 RX

K-Number: K961809 · 1997-02-26

Decision Date1997-02-26
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

SHE-LI TENS STIMULATOR MODEL SL-101 RX is the device name listed in this FDA 510(k) record. The listed applicant is Medi Consultants, Inc.. It received FDA 510(k) clearance on 1997-02-26 under 510(k) number K961809. 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 SHE-LI TENS STIMULATOR MODEL SL-101 RX?

SHE-LI TENS STIMULATOR MODEL SL-101 RX is a medical device that received FDA 510(k) clearance on 1997-02-26. The listed applicant is Medi Consultants, Inc.. The 510(k) number is K961809.

When did SHE-LI TENS STIMULATOR MODEL SL-101 RX receive FDA 510(k) clearance?

SHE-LI TENS STIMULATOR MODEL SL-101 RX received FDA 510(k) clearance on 1997-02-26, under 510(k) number K961809.

Who is the listed applicant for SHE-LI TENS STIMULATOR MODEL SL-101 RX?

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

What is the FDA product code for SHE-LI TENS STIMULATOR MODEL SL-101 RX?

The FDA product code for SHE-LI TENS STIMULATOR MODEL SL-101 RX 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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