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MODEL E 600 ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K860767
510(k) Type
Traditional
Applicant
KONE INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/1986
Days to Decision
51 days

MODEL E 600 ELECTROCARDIOGRAPH

Page Type
Cleared 510(K)
510(k) Number
K860767
510(k) Type
Traditional
Applicant
KONE INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/23/1986
Days to Decision
51 days