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MODEL 2100 FETAL MONITOR

Page Type
Cleared 510(K)
510(k) Number
K837102
510(k) Type
Traditional
Applicant
HUNTLEIGH GROUP LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/14/1983
Days to Decision
66 days

MODEL 2100 FETAL MONITOR

Page Type
Cleared 510(K)
510(k) Number
K837102
510(k) Type
Traditional
Applicant
HUNTLEIGH GROUP LTD.
Country
United Kingdom
FDA Decision
Substantially Equivalent
Decision Date
3/14/1983
Days to Decision
66 days