ELECTROSTIMULATOR MODEL 808— 510(k) K880426

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..

Clearance details

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

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