MICROSTIM 100I TENS DEVICE— 510(k) K010295

Substantially Equivalent

Microstim, Inc.

FDA 510(k) clearance K010295 for MICROSTIM 100I TENS DEVICE, Substantially Equivalent on 2001-08-03. Applicant: Microstim, Inc.. Device class: 2.

Clearance details

Applicant: Microstim, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2001-01-31
Decision date: 2001-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tamarac, FL, US

Download summary PDF View on FDA.gov ↗

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