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LinkQuest Diagnostic Ultrasound System model SQ860

Page Type
Cleared 510(K)
510(k) Number
K172059
510(k) Type
Traditional
Applicant
LinkQuest Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2017
Days to Decision
90 days
Submission Type
Summary

LinkQuest Diagnostic Ultrasound System model SQ860

Page Type
Cleared 510(K)
510(k) Number
K172059
510(k) Type
Traditional
Applicant
LinkQuest Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2017
Days to Decision
90 days
Submission Type
Summary