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NICOLET EMG SATELLITE

Page Type
Cleared 510(K)
510(k) Number
K830702
510(k) Type
Traditional
Applicant
NICOLET BIOMEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1983
Days to Decision
127 days

NICOLET EMG SATELLITE

Page Type
Cleared 510(K)
510(k) Number
K830702
510(k) Type
Traditional
Applicant
NICOLET BIOMEDICAL INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/1983
Days to Decision
127 days