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PROFESSIONAL SERIES BIOFEEDBACK DEVICES MODEL 421

Page Type
Cleared 510(K)
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)
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