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Site-Rite 8 Ultrasound System, Site-Rite 8 Ultrasound System with Pinpoint GT Technology

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152554
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2015
Days to Decision
97 days
Submission Type
Summary

Site-Rite 8 Ultrasound System, Site-Rite 8 Ultrasound System with Pinpoint GT Technology

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152554
510(k) Type
Traditional
Applicant
C.R. Bard, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/14/2015
Days to Decision
97 days
Submission Type
Summary