DORMIE NECK SUPPORT SYSTEM— 510(k) K930730

Name: FDA 510(k) clearance K930730
Creator: U.S. Food and Drug Administration
Published: 1993-07-22

Substantially Equivalent

The Western Diagnostics Co.

FDA 510(k) clearance K930730 for DORMIE NECK SUPPORT SYSTEM, Substantially Equivalent on 1993-07-22. Applicant: The Western Diagnostics Co.. Device class: 1.

Clearance details

Applicant: The Western Diagnostics Co.
Product code: Code IQK
Device class: Class 1
Regulation: 21 CFR 890.3490
Advisory panel: Physical Medicine
Date received: 1993-02-11
Decision date: 1993-07-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Palm Beach, FL, 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.