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BIOCOMP 2001 BIOFEEDBACK DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872495
510(k) Type
Traditional
Applicant
BIOFEEDBACK RESEARCH INSTITUTE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1987
Days to Decision
41 days

BIOCOMP 2001 BIOFEEDBACK DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K872495
510(k) Type
Traditional
Applicant
BIOFEEDBACK RESEARCH INSTITUTE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/4/1987
Days to Decision
41 days