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MODEL K7 EVALUATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003287
510(k) Type
Special
Applicant
MYOTRONICS-NOROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2000
Days to Decision
17 days
Submission Type
Summary

MODEL K7 EVALUATION DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003287
510(k) Type
Special
Applicant
MYOTRONICS-NOROMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2000
Days to Decision
17 days
Submission Type
Summary