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ECG SIMULATOR MODEL ECGPLUS

Page Type
Cleared 510(K)
510(k) Number
K893660
510(k) Type
Traditional
Applicant
BIO-TEK INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/1989
Days to Decision
204 days

ECG SIMULATOR MODEL ECGPLUS

Page Type
Cleared 510(K)
510(k) Number
K893660
510(k) Type
Traditional
Applicant
BIO-TEK INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/1989
Days to Decision
204 days