ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM— 510(k) K892114

Name: FDA 510(k) clearance K892114
Creator: U.S. Food and Drug Administration
Published: 1989-10-13

Substantially Equivalent

Eclosion, Inc.

FDA 510(k) clearance K892114 for ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM, Substantially Equivalent on 1989-10-13. Applicant: Eclosion, Inc.. Device class: 2.

Clearance details

Applicant: Eclosion, Inc.
Product code: Code HCC
Device class: Class 2
Regulation: 21 CFR 882.5050
Advisory panel: Neurology
Date received: 1989-03-30
Decision date: 1989-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denver, CO, US

Download summary PDF View on FDA.gov ↗

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