Acuson Picture Archiving & Communication System Modification

FDA 510(k) K940285 · Acuson Corp.

Substantially Equivalent

510(k) numberK940285

Submission

Device name
Acuson Picture Archiving & Communication System Modification
Applicant
Acuson Corp.
Mountain View, CA, US
Received
January 10, 1994
Decision date
April 29, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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 Acuson Picture Archiving & Communication System Modification cleared by the FDA?

Acuson Picture Archiving & Communication System Modification (K940285) received a 510(k) decision of Substantially Equivalent on April 29, 1994, 109 days after the submission was received.

What is the product code of K940285?

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