510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K880839Substantially Equivalent

Ai 5200 Diagnostic Ultrasound System

Phoenix Imaging, Tempe AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K880839 is the FDA 510(k) clearance record for AI 5200 DIAGNOSTIC ULTRASOUND SYSTEM, a class II device, cleared for Phoenix Imaging on under FDA product code IYO (System, Imaging, Pulsed Echo, Ultrasonic). FDA records list 2 510(k) clearances for Phoenix Imaging, from to . As of , FDA records show no recalls naming K880839.

Clearance record

Decision date
Received
(101 days to decision)
Product code
IYO System, Imaging, Pulsed Echo, Ultrasonic
Regulation
21 CFR 892.1560
Device class
Class II
Review panel
Radiology
Applicant
Phoenix Imaging 4666 S. Ash Ave., Tempe AZ
Third party review
No

Clearances, product code IYO

Trailing 12 months
8 clearances under product code IYO in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code IYO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20262
March 20261
April 20262
May 20260
June 20261
July 20261
August 20260
September 20261
October 20260