CONTRAST 7000 THERAPY SYSTEM— 510(k) K943497

Name: FDA 510(k) clearance K943497
Creator: U.S. Food and Drug Administration
Published: 1995-06-07

Substantially Equivalent

Burke Neutech, Inc.

FDA 510(k) clearance K943497 for CONTRAST 7000 THERAPY SYSTEM, Substantially Equivalent on 1995-06-07. Applicant: Burke Neutech, Inc.. Device class: 2.

Clearance details

Applicant: Burke Neutech, Inc.
Product code: Code ILO
Device class: Class 2
Regulation: 21 CFR 890.5720
Advisory panel: Physical Medicine
Date received: 1994-07-19
Decision date: 1995-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Largo, FL, US

Download summary PDF View on FDA.gov ↗

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