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HTS 820 CARDIAC MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896967
510(k) Type
Traditional
Applicant
LIFE SENSING INSTRUMENT COMPANY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1990
Days to Decision
91 days

HTS 820 CARDIAC MONITOR

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K896967
510(k) Type
Traditional
Applicant
LIFE SENSING INSTRUMENT COMPANY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/19/1990
Days to Decision
91 days