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NEUROMETER

Page Type
Cleared 510(K)
510(k) Number
K853608
510(k) Type
Traditional
Applicant
NEUROTRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1986
Days to Decision
288 days

NEUROMETER

Page Type
Cleared 510(K)
510(k) Number
K853608
510(k) Type
Traditional
Applicant
NEUROTRON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/1986
Days to Decision
288 days