SHE-LI TENS STIMULATOR MODEL SL-101 RX
K-Number: K961809 · 1997-02-26
Advertisement
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement