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PATIENT MONITOR #RM-100

Page Type
Cleared 510(K)
510(k) Number
K831817
510(k) Type
Traditional
Applicant
HONEYWELL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/1983
Days to Decision
147 days

PATIENT MONITOR #RM-100

Page Type
Cleared 510(K)
510(k) Number
K831817
510(k) Type
Traditional
Applicant
HONEYWELL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/31/1983
Days to Decision
147 days