Last synced on 30 September 2022 at 11:05 pm

MODEL MES-9000/EMG SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013399
510(k) Type
Special
Applicant
MYOTRONICS-NOROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2001
Days to Decision
29 days
Submission Type
Summary

MODEL MES-9000/EMG SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013399
510(k) Type
Special
Applicant
MYOTRONICS-NOROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/13/2001
Days to Decision
29 days
Submission Type
Summary