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PERIPHERAL NERVE STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760614
510(k) Type
Traditional
Applicant
OUTPUT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1976
Days to Decision
70 days

PERIPHERAL NERVE STIMULATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K760614
510(k) Type
Traditional
Applicant
OUTPUT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/1976
Days to Decision
70 days