ELECTROSTIMULATOR MODEL 808— 510(k) K880426

Name: FDA 510(k) clearance K880426
Creator: U.S. Food and Drug Administration
Published: 1988-09-19

Substantially Equivalent

Cornell Enterprises Co., Inc.

FDA 510(k) clearance K880426 for ELECTROSTIMULATOR MODEL 808, Substantially Equivalent on 1988-09-19. Applicant: Cornell Enterprises Co., Inc.. Device class: 2.

Clearance details

Applicant: Cornell Enterprises Co., Inc.
Product code: Code GZJ
Device class: Class 2
Regulation: 21 CFR 882.5890
Advisory panel: Neurology
Date received: 1988-02-01
Decision date: 1988-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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