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Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech

Page Type
Cleared 510(K)
510(k) Number
K182281
510(k) Type
Traditional
Applicant
C.R. Bard
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2018
Days to Decision
62 days
Submission Type
Summary

Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech

Page Type
Cleared 510(K)
510(k) Number
K182281
510(k) Type
Traditional
Applicant
C.R. Bard
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/24/2018
Days to Decision
62 days
Submission Type
Summary