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M2100 ANTEPARTUM FETAL MONITOR

Page Type
Cleared 510(K)
510(k) Number
K823081
510(k) Type
Traditional
Applicant
HUNTLEIGH TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1983
Days to Decision
99 days

M2100 ANTEPARTUM FETAL MONITOR

Page Type
Cleared 510(K)
510(k) Number
K823081
510(k) Type
Traditional
Applicant
HUNTLEIGH TECHNOLOGY, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1983
Days to Decision
99 days