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EMG MODULE, EMG1, W/OPTIONAL SPEAKER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842124
510(k) Type
Traditional
Applicant
ENDOTEK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/1984
Days to Decision
71 days

EMG MODULE, EMG1, W/OPTIONAL SPEAKER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K842124
510(k) Type
Traditional
Applicant
ENDOTEK CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/8/1984
Days to Decision
71 days