Hdi 5000 Ultrasound System with Extended Field of View Imaging

FDA 510(k) K002003 · Atl Ultrasound, Inc.

Substantially Equivalent

510(k) numberK002003

Submission

Device name
Hdi 5000 Ultrasound System with Extended Field of View Imaging
Applicant
Atl Ultrasound, Inc.
Bothell, WA, US
Received
June 30, 2000
Decision date
July 13, 2000
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 Hdi 5000 Ultrasound System with Extended Field of View Imaging cleared by the FDA?

Hdi 5000 Ultrasound System with Extended Field of View Imaging (K002003) received a 510(k) decision of Substantially Equivalent on July 13, 2000, 13 days after the submission was received.

What is the product code of K002003?

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