Last synced on 25 April 2025 at 11:05 pm

LinkQuest Diagnostic Ultrasound System model SQ860

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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