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ABDOMINAL ECG PROCESSOR FOR FETAL MONI.

Page Type
Cleared 510(K)
510(k) Number
K770295
510(k) Type
Traditional
Applicant
BRATTLE INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1977
Days to Decision
23 days

ABDOMINAL ECG PROCESSOR FOR FETAL MONI.

Page Type
Cleared 510(K)
510(k) Number
K770295
510(k) Type
Traditional
Applicant
BRATTLE INSTRUMENT CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1977
Days to Decision
23 days