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Acclarix LX8 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162055
510(k) Type
Traditional
Applicant
EDAN INSTRUMENTS INC
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/31/2017
Days to Decision
190 days
Submission Type
Summary

Acclarix LX8 Diagnostic Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162055
510(k) Type
Traditional
Applicant
EDAN INSTRUMENTS INC
Country
China
FDA Decision
Substantially Equivalent
Decision Date
1/31/2017
Days to Decision
190 days
Submission Type
Summary