Last synced on 15 September 2023 at 11:04 pm

EMG REPORT GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K844681
510(k) Type
Traditional
Applicant
MICROSYSTEM CONTROLS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1985
Days to Decision
88 days

EMG REPORT GENERATOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K844681
510(k) Type
Traditional
Applicant
MICROSYSTEM CONTROLS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/26/1985
Days to Decision
88 days