Last synced on 14 November 2025 at 11:06 pm

Fetal EchoScan

Page Type
Cleared 510(K)
510(k) Number
K242342
510(k) Type
Traditional
Applicant
BrightHeart
Country
France
FDA Decision
Substantially Equivalent
Decision Date
11/14/2024
Days to Decision
99 days
Submission Type
Summary

Fetal EchoScan

Page Type
Cleared 510(K)
510(k) Number
K242342
510(k) Type
Traditional
Applicant
BrightHeart
Country
France
FDA Decision
Substantially Equivalent
Decision Date
11/14/2024
Days to Decision
99 days
Submission Type
Summary