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PATHFINDER ELECTRODIAGNOSTIC SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K801604
510(k) Type
Traditional
Applicant
NICOLET BIOMEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1980
Days to Decision
21 days

PATHFINDER ELECTRODIAGNOSTIC SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K801604
510(k) Type
Traditional
Applicant
NICOLET BIOMEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1980
Days to Decision
21 days