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LME BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K832017
510(k) Type
Traditional
Applicant
LITTON MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/1983
Days to Decision
130 days

LME BLOOD PRESSURE MONITOR

Page Type
Cleared 510(K)
510(k) Number
K832017
510(k) Type
Traditional
Applicant
LITTON MEDICAL ELECTRONICS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/1983
Days to Decision
130 days