510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K033238Substantially Equivalent

Mobilette Xp and Mobilett Xphybrid

Siemens Medical Solutions USA, Inc., Mavern PA / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K033238 is the FDA 510(k) clearance record for MOBILETTE XP AND MOBILETT XPHYBRID, a class II device, cleared for Siemens Medical Systems, Inc. on under FDA product code IZL (System, X-Ray, Mobile). FDA records list 829 510(k) clearances for SIEMENS MEDICAL SOLUTIONS USA, INC., from to . As of , FDA records show 4 recalls naming K033238.

Clearance record

Decision date
Received
(39 days to decision)
Product code
IZL System, X-Ray, Mobile
Regulation
21 CFR 892.1720
Device class
Class II
Review panel
Radiology
Applicant
Siemens Medical Systems, Inc. 51 Valley Stream Pkwy., Mavern PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IZL

Trailing 12 months
6 clearances under product code IZL in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code IZL, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20261
March 20261
April 20260
May 20261
June 20261
July 20260
August 20261
September 20260
October 20260