PATHFINDER ELECTRODIAGNOSTIC SYSTEM— 510(k) K801604

Substantially Equivalent

Nicolet Biomedical Instruments

FDA 510(k) clearance K801604 for PATHFINDER ELECTRODIAGNOSTIC SYSTEM, Substantially Equivalent on 1980-08-04. Applicant: Nicolet Biomedical Instruments.

Clearance details

Applicant: Nicolet Biomedical Instruments
Product code: Code GWK
Advisory panel: Neurology
Date received: 1980-07-14
Decision date: 1980-08-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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