Last synced on 4 February 2023 at 10:33 pm

MYOTONE EMG MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K772005
510(k) Type
Traditional
Applicant
MICROTRONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1977
Days to Decision
33 days

MYOTONE EMG MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K772005
510(k) Type
Traditional
Applicant
MICROTRONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/23/1977
Days to Decision
33 days