INTER TRON 4000— 510(k) K880924

Name: FDA 510(k) clearance K880924
Creator: U.S. Food and Drug Administration
Published: 1988-10-13

Substantially Equivalent

Diversified Chiropractic Systems

FDA 510(k) clearance K880924 for INTER TRON 4000, Substantially Equivalent on 1988-10-13. Applicant: Diversified Chiropractic Systems. Device class: 2.

Clearance details

Applicant: Diversified Chiropractic Systems
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1988-03-04
Decision date: 1988-10-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Olathe, KS, US

Download summary PDF View on FDA.gov ↗

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