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EVENTMASTER 2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820856
510(k) Type
Traditional
Applicant
INSTRUMENTS FOR CARDIAC RESEARCH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1982
Days to Decision
31 days

EVENTMASTER 2

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K820856
510(k) Type
Traditional
Applicant
INSTRUMENTS FOR CARDIAC RESEARCH
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1982
Days to Decision
31 days