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BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884852
510(k) Type
Traditional
Applicant
MOE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1989
Days to Decision
76 days

BIOFEEDBACK DEVICE EMG1, EMG ULTRA LOW NOISE OPTI.

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K884852
510(k) Type
Traditional
Applicant
MOE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/1989
Days to Decision
76 days