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FETALGARD 3000 FETAL MONITOR

Page Type
Cleared 510(K)
510(k) Number
K983395
510(k) Type
Traditional
Applicant
ANALOGIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1999
Days to Decision
321 days
Submission Type
Summary

FETALGARD 3000 FETAL MONITOR

Page Type
Cleared 510(K)
510(k) Number
K983395
510(k) Type
Traditional
Applicant
ANALOGIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/12/1999
Days to Decision
321 days
Submission Type
Summary