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MORTARA ELI 350 ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K082946
510(k) Type
Traditional
Applicant
MORTARA INSTRUMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/2008
Days to Decision
88 days
Submission Type
Summary

MORTARA ELI 350 ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K082946
510(k) Type
Traditional
Applicant
MORTARA INSTRUMENT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/2008
Days to Decision
88 days
Submission Type
Summary