SHE-LI TENS STIMULATOR MODEL SL-101 RX— 510(k) K961809

Name: FDA 510(k) clearance K961809
Creator: U.S. Food and Drug Administration
Published: 1997-02-26

Substantially Equivalent

Medi Consultants, Inc.

FDA 510(k) clearance K961809 for SHE-LI TENS STIMULATOR MODEL SL-101 RX, Substantially Equivalent on 1997-02-26. Applicant: Medi Consultants, Inc.. Device class: 2.

Clearance details

Applicant: Medi Consultants, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1996-05-10
Decision date: 1997-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paterson, NJ, US

Download summary PDF View on FDA.gov ↗

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