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MODEL 2106 FETA SONDE FETAL MONITOR

Page Type
Cleared 510(K)
510(k) Number
K760919
510(k) Type
Traditional
Applicant
ROCHE MEDICAL ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1976
Days to Decision
19 days

MODEL 2106 FETA SONDE FETAL MONITOR

Page Type
Cleared 510(K)
510(k) Number
K760919
510(k) Type
Traditional
Applicant
ROCHE MEDICAL ELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/16/1976
Days to Decision
19 days