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PROFESSIONAL SERIES BIOFEEDBACK DEVICES MODEL 421

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K875308
510(k) Type
Traditional
Applicant
SELF REGULATION SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1988
Days to Decision
59 days

PROFESSIONAL SERIES BIOFEEDBACK DEVICES MODEL 421

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K875308
510(k) Type
Traditional
Applicant
SELF REGULATION SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1988
Days to Decision
59 days