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SITE RITE PREVUE ULTRASOUND SYSTEM AND PINPOINT NEEDLE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K120882
510(k) Type
Traditional
Applicant
BARD ACCESS SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2012
Days to Decision
68 days
Submission Type
Summary

SITE RITE PREVUE ULTRASOUND SYSTEM AND PINPOINT NEEDLE GUIDE

Page Type
Cleared 510(K)
510(k) Number
K120882
510(k) Type
Traditional
Applicant
BARD ACCESS SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/30/2012
Days to Decision
68 days
Submission Type
Summary