Last synced on 14 November 2025 at 11:06 pm

ADDITIONAL SOFTWARE TO CARDIODYNAMIC MONITOR

Page Type
Cleared 510(K)
510(k) Number
K890408
510(k) Type
Traditional
Applicant
BOMED MEDICAL MFG., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1989
Days to Decision
128 days

ADDITIONAL SOFTWARE TO CARDIODYNAMIC MONITOR

Page Type
Cleared 510(K)
510(k) Number
K890408
510(k) Type
Traditional
Applicant
BOMED MEDICAL MFG., LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/1989
Days to Decision
128 days