510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K072918Substantially Equivalent

Model Ssa-680A Xario Xg Diagnostic Ultrasound System, Version 1.00

Toshibamedical Systems Corporation, Tustin CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K072918 is the FDA 510(k) clearance record for MODEL SSA-680A XARIO XG DIAGNOSTIC ULTRASOUND SYSTEM, VERSION 1.00, a class II device, cleared for Toshibamedical Systems Corporation on under FDA product code ITX (Transducer, Ultrasonic, Diagnostic). FDA records list 80 510(k) clearances for Toshibamedical Systems Corporation, from to . As of , FDA records show 3 recalls naming K072918.

Clearance record

Decision date
Received
(14 days to decision)
Product code
ITX Transducer, Ultrasonic, Diagnostic
Regulation
21 CFR 892.1570
Device class
Class II
Review panel
Radiology
Applicant
Toshibamedical Systems Corporation 2441 Michelle Dr., Tustin CA
510(k) summary
Summary PDF
Third party review
Yes

Clearances, product code ITX

Trailing 12 months
6 clearances under product code ITX in the twelve months to October 2026, July 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code ITX, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20263
August 20262
September 20261
October 20260