510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935694Substantially Equivalent

Sienet Diagnostic Reporting Console Va02 Upgrade

Siemens Medical Solutions USA, Inc., Iselin NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935694 is the FDA 510(k) clearance record for SIENET DIAGNOSTIC REPORTING CONSOLE VA02 UPGRADE, a class II device, cleared for Siemens Medical Solutions USA, Inc. on under FDA product code LLZ (System, Image Processing, Radiological). FDA records list 829 510(k) clearances for Siemens Medical Solutions USA, Inc., from to . As of , FDA records show 4 recalls naming K935694.

Clearance record

Decision date
Received
(98 days to decision)
Product code
LLZ System, Image Processing, Radiological
Regulation
21 CFR 892.2050
Device class
Class II
Review panel
Radiology
Applicant
Siemens Medical Solutions USA, Inc. 186 Wood Ave. S., Iselin NJ
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