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DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K913595
510(k) Type
Traditional
Applicant
KOVEN AND ASSOC., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1992
Days to Decision
227 days
Submission Type
Statement

DS-240 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K913595
510(k) Type
Traditional
Applicant
KOVEN AND ASSOC., INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/27/1992
Days to Decision
227 days
Submission Type
Statement