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LIGHTMED Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K183173
510(k) Type
Traditional
Applicant
Lightmed USA, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2019
Days to Decision
227 days
Submission Type
Summary

LIGHTMED Ultrasound System

Page Type
Cleared 510(K)
510(k) Number
K183173
510(k) Type
Traditional
Applicant
Lightmed USA, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/2019
Days to Decision
227 days
Submission Type
Summary