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PACEART CARDIOPHONE

Page Type
Cleared 510(K)
510(k) Number
K931296
510(k) Type
Traditional
Applicant
PACEART, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1993
Days to Decision
185 days
Submission Type
Summary

PACEART CARDIOPHONE

Page Type
Cleared 510(K)
510(k) Number
K931296
510(k) Type
Traditional
Applicant
PACEART, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/1/1993
Days to Decision
185 days
Submission Type
Summary