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BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884849
510(k) Type
Traditional
Applicant
MOE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1989
Days to Decision
125 days

BIOFEEDBACK DEVICE ACCESS. PI1,2,3,4,5/LIGHT BAR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884849
510(k) Type
Traditional
Applicant
MOE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/23/1989
Days to Decision
125 days