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MODEL S10VS VISUAL STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812061
510(k) Type
Traditional
Applicant
GRASS INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1981
Days to Decision
30 days

MODEL S10VS VISUAL STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812061
510(k) Type
Traditional
Applicant
GRASS INSTRUMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/20/1981
Days to Decision
30 days