Last synced on 14 November 2025 at 11:06 pm

HTS 220 CARDIAC MONITOR

Page Type
Cleared 510(K)
510(k) Number
K884524
510(k) Type
Traditional
Applicant
LIFE SENSING INSTRUMENT COMPANY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1989
Days to Decision
165 days

HTS 220 CARDIAC MONITOR

Page Type
Cleared 510(K)
510(k) Number
K884524
510(k) Type
Traditional
Applicant
LIFE SENSING INSTRUMENT COMPANY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/10/1989
Days to Decision
165 days