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SiteRite™ 9 Ultrasound System

Page Type
Cleared 510(K)
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)
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