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AMBULATORY BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K873764
510(k) Type
Traditional
Applicant
PULSETREND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1988
Days to Decision
268 days

AMBULATORY BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K873764
510(k) Type
Traditional
Applicant
PULSETREND, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/10/1988
Days to Decision
268 days