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MODIFICATION TO FETAL ASSIST

Page Type
Cleared 510(K)
510(k) Number
K020390
510(k) Type
Traditional
Applicant
Huntleigh Diagnostics , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2002
Days to Decision
72 days
Submission Type
Summary

MODIFICATION TO FETAL ASSIST

Page Type
Cleared 510(K)
510(k) Number
K020390
510(k) Type
Traditional
Applicant
Huntleigh Diagnostics , Ltd.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/19/2002
Days to Decision
72 days
Submission Type
Summary