ANASTIM II TRANSCUTANEOUS ELECTRICAL— 510(k) K802227

Name: FDA 510(k) clearance K802227
Creator: U.S. Food and Drug Administration
Published: 1980-09-26

Substantially Equivalent

Biostim, Inc.

FDA 510(k) clearance K802227 for ANASTIM II TRANSCUTANEOUS ELECTRICAL, Substantially Equivalent on 1980-09-26. Applicant: Biostim, Inc.. Device class: 2.

Clearance details

Applicant: Biostim, Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1980-09-12
Decision date: 1980-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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