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LME HEART-RATE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K832016
510(k) Type
Traditional
Applicant
LITTON MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1983
Days to Decision
125 days

LME HEART-RATE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K832016
510(k) Type
Traditional
Applicant
LITTON MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/26/1983
Days to Decision
125 days