Last synced on 14 November 2025 at 11:06 pm

Lumify Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K203406
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2021
Days to Decision
96 days
Submission Type
Summary

Lumify Diagnostic Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K203406
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/23/2021
Days to Decision
96 days
Submission Type
Summary