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MODEL M402 EMG MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864660
510(k) Type
Traditional
Applicant
BIO-LOGIC DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1987
Days to Decision
68 days

MODEL M402 EMG MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K864660
510(k) Type
Traditional
Applicant
BIO-LOGIC DEVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/4/1987
Days to Decision
68 days