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P.H.D. - PERSONAL HEART DEVICE MODEL 5258

Page Type
Cleared 510(K)
510(k) Number
K963904
510(k) Type
Traditional
Applicant
HEART ALERT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1997
Days to Decision
227 days
Submission Type
Statement

P.H.D. - PERSONAL HEART DEVICE MODEL 5258

Page Type
Cleared 510(K)
510(k) Number
K963904
510(k) Type
Traditional
Applicant
HEART ALERT, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/1997
Days to Decision
227 days
Submission Type
Statement