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SiteRite™ 9 Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231283
510(k) Type
Traditional
Applicant
Bard Access Systems, Inc. (C.R. Bard, Inc.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2023
Days to Decision
131 days
Submission Type
Summary

SiteRite™ 9 Ultrasound System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231283
510(k) Type
Traditional
Applicant
Bard Access Systems, Inc. (C.R. Bard, Inc.)
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2023
Days to Decision
131 days
Submission Type
Summary