ELECTROSTIMULI AVERSION MACHINE— 510(k) K820622

Name: FDA 510(k) clearance K820622
Creator: U.S. Food and Drug Administration
Published: 1982-04-09

Substantially Equivalent

Michael R. Kiss

FDA 510(k) clearance K820622 for ELECTROSTIMULI AVERSION MACHINE, Substantially Equivalent on 1982-04-09. Applicant: Michael R. Kiss. Device class: 2.

Clearance details

Applicant: Michael R. Kiss
Product code: Code HCB
Device class: Class 2
Regulation: 21 CFR 882.5235
Advisory panel: Neurology
Date received: 1982-03-08
Decision date: 1982-04-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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