TENS— 510(k) K921110

Substantially Equivalent

Staodyne, Inc.

FDA 510(k) clearance K921110 for TENS, Substantially Equivalent on 1992-08-14. Applicant: Staodyne, Inc.. Device class: 2.

Clearance details

Applicant: Staodyne, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1992-03-09
Decision date: 1992-08-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Longmont, CO, US

Download summary PDF View on FDA.gov ↗

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More clearances from Staodyne, Inc.

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K931424 — MAXIMA I1993-06-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.