Last synced on 30 September 2022 at 11:05 pm

FEEDBACK EMG SYSTEM, MODEL PE-L00

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770663
510(k) Type
Traditional
Applicant
BIO-FEEDBACK SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1977
Days to Decision
19 days

FEEDBACK EMG SYSTEM, MODEL PE-L00

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K770663
510(k) Type
Traditional
Applicant
BIO-FEEDBACK SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/1977
Days to Decision
19 days