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NEUROSTIM II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822138
510(k) Type
Traditional
Applicant
NEURO TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1982
Days to Decision
11 days

NEUROSTIM II

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822138
510(k) Type
Traditional
Applicant
NEURO TECHNOLOGY
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1982
Days to Decision
11 days