THE CAROLINA ROCKER— 510(k) K900839

Name: FDA 510(k) clearance K900839
Creator: U.S. Food and Drug Administration
Published: 1990-04-18

Substantially Equivalent

Artec Environmental Monitoring Division

FDA 510(k) clearance K900839 for THE CAROLINA ROCKER, Substantially Equivalent on 1990-04-18. Applicant: Artec Environmental Monitoring Division. Device class: 1.

Clearance details

Applicant: Artec Environmental Monitoring Division
Product code: Code KNN
Device class: Class 1
Regulation: 21 CFR 890.3920
Advisory panel: Physical Medicine
Date received: 1990-02-22
Decision date: 1990-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Greenville, SC, US

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