Last synced on 14 November 2025 at 11:06 pm

KANTRON 504 HEARTSTATION

Page Type
Cleared 510(K)
510(k) Number
K812586
510(k) Type
Traditional
Applicant
KANTRON CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1981
Days to Decision
109 days

KANTRON 504 HEARTSTATION

Page Type
Cleared 510(K)
510(k) Number
K812586
510(k) Type
Traditional
Applicant
KANTRON CARDIOVASCULAR, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/29/1981
Days to Decision
109 days