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NEUROPLUS, MODEL A10040, A10041, A10042, A10043

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010638
510(k) Type
Traditional
Applicant
Vermont Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2001
Days to Decision
59 days
Submission Type
Statement

NEUROPLUS, MODEL A10040, A10041, A10042, A10043

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K010638
510(k) Type
Traditional
Applicant
Vermont Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/3/2001
Days to Decision
59 days
Submission Type
Statement