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PHOTRON NEUROVISUAL STIMULATOR(MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853812
510(k) Type
Traditional
Applicant
BIOSAN LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1985
Days to Decision
50 days

PHOTRON NEUROVISUAL STIMULATOR(MODIFICATION)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K853812
510(k) Type
Traditional
Applicant
BIOSAN LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/1/1985
Days to Decision
50 days