510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K962589Substantially Equivalent

Aurora Diagnostic Workstation

Aurora Technology Pte. Ltd., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K962589 is the FDA 510(k) clearance record for AURORA DIAGNOSTIC WORKSTATION, a class II device, cleared for Aurora Technology, Inc. on under FDA product code LLZ (System, Image Processing, Radiological). FDA records list one 510(k) clearance for Aurora Technology, Inc. As of , FDA records show no recalls naming K962589.

Clearance record

Decision date
Received
(80 days to decision)
Product code
LLZ System, Image Processing, Radiological
Regulation
21 CFR 892.2050
Device class
Class II
Review panel
Radiology
Applicant
Aurora Technology, Inc. 10560 Wayzata Blvd., Minneapolis MN
510(k) summary
Summary
Third party review
No

Clearances, product code LLZ

Trailing 12 months
47 clearances under product code LLZ in the twelve months to October 2026, July 2026 the highest month at 8.
Show the numbers
Monthly 510(k) clearances under FDA product code LLZ, trailing twelve months
MonthClearances
November 20254
December 20251
January 20263
February 20264
March 20266
April 20262
May 20265
June 20265
July 20268
August 20263
September 20266
October 20260