FDA 510(k)

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

Numéro K : K182281 · 2018-10-24

Date de décision2018-10-24

Code produitIYO

Comité consultatifRA

DécisionSubstantially Equivalent

Résumé du dispositif

Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech is the device name listed in this FDA 510(k) record. The listed applicant is C. R. Bard. It received FDA 510(k) clearance on 2018-10-24 under 510(k) number K182281. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Questions fréquentes

What is the Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech?

Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech is a medical device that received FDA 510(k) clearance on 2018-10-24. The listed applicant is C. R. Bard. The 510(k) number is K182281.

When did Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech receive FDA 510(k) clearance?

Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech received FDA 510(k) clearance on 2018-10-24, under 510(k) number K182281.

Who is the listed applicant for Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech?

The FDA 510(k) record lists C. R. Bard as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech?

The FDA product code for Site~Rite 8 Ultrasound System with Cue Needle Tracking System and Pinpoint GT Needle Tech is IYO.

Essais cliniques associés

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Source officielle

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