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FETAL & MATERNAL MONITOR, MODEL F6, F9

Page Type
Cleared 510(K)
510(k) Number
K082602
510(k) Type
Traditional
Applicant
EDAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2008
Days to Decision
79 days
Submission Type
Summary

FETAL & MATERNAL MONITOR, MODEL F6, F9

Page Type
Cleared 510(K)
510(k) Number
K082602
510(k) Type
Traditional
Applicant
EDAN INSTRUMENTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/26/2008
Days to Decision
79 days
Submission Type
Summary