Last synced on 10 January 2025 at 11:05 pm

M424 EMG MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880913
510(k) Type
Traditional
Applicant
BIO-LOGIC DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1988
Days to Decision
69 days

M424 EMG MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K880913
510(k) Type
Traditional
Applicant
BIO-LOGIC DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/11/1988
Days to Decision
69 days