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EME MP3000 MONITORING AND DIAGNOSTIC RESTING ECG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920867
510(k) Type
Traditional
Applicant
ELECTRO MEDICAL EQUIPMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1992
Days to Decision
45 days
Submission Type
Statement

EME MP3000 MONITORING AND DIAGNOSTIC RESTING ECG

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920867
510(k) Type
Traditional
Applicant
ELECTRO MEDICAL EQUIPMENT CO., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1992
Days to Decision
45 days
Submission Type
Statement