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PACEART TX3 CARDIAC EVENT RECORDER

Page Type
Cleared 510(K)
510(k) Number
K012407
510(k) Type
Special
Applicant
PACEART, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2001
Days to Decision
15 days
Submission Type
Summary

PACEART TX3 CARDIAC EVENT RECORDER

Page Type
Cleared 510(K)
510(k) Number
K012407
510(k) Type
Special
Applicant
PACEART, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2001
Days to Decision
15 days
Submission Type
Summary