Site-Rite Vision Ultrasound System

FDA 510(k) K100402 · Bard Access Systems, Inc.

Substantially Equivalent

510(k) numberK100402

Submission

Device name
Site-Rite Vision Ultrasound System
Applicant
Bard Access Systems, Inc.
Salt Lake Ciy,, UT, US
Received
February 16, 2010
Decision date
March 5, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
IYN – System, Imaging, Pulsed Doppler, Ultrasonic
Device class
Class II (moderate risk)
Regulation
21 CFR 892.1550
Specialty
Radiology

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Questions and answers

When was Site-Rite Vision Ultrasound System cleared by the FDA?

Site-Rite Vision Ultrasound System (K100402) received a 510(k) decision of Substantially Equivalent on March 5, 2010, 17 days after the submission was received.

What is the product code of K100402?

The FDA product code is IYN – System, Imaging, Pulsed Doppler, Ultrasonic, a Class II (moderate risk) device regulated under 21 CFR 892.1550.