CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000— 510(k) K033358

Name: FDA 510(k) clearance K033358
Creator: U.S. Food and Drug Administration
Published: 2003-11-14

Substantially Equivalent

Surgitech, Inc.

FDA 510(k) clearance K033358 for CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000, Substantially Equivalent on 2003-11-14. Applicant: Surgitech, Inc.. Device class: 2.

Clearance details

Applicant: Surgitech, Inc.
Product code: Code LIH
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 2003-10-20
Decision date: 2003-11-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Oceanside, CA, US

Download summary PDF View on FDA.gov ↗

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