510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K203346Substantially Equivalent

Oec 3D

GE Healthcare, Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K203346 is the FDA 510(k) clearance record for OEC 3D, a class II device, cleared for Ge Oec Medical Systems, Inc. on under FDA product code OXO (Image-Intensified Fluoroscopic X-Ray System, Mobile). FDA's definition for product code OXO reads: "Fluoroscopy of the human body". FDA records list 888 510(k) clearances for GE HEALTHCARE, from to . As of , FDA records show 3 recalls naming K203346.

Clearance record

Decision date
Received
(112 days to decision)
Product code
OXO Image-Intensified Fluoroscopic X-Ray System, Mobile
Regulation
21 CFR 892.1650
Device class
Class II
Review panel
Radiology
Applicant
Ge Oec Medical Systems, Inc. 384 N Wright Brothers Dr., Salt Lake City UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OXO

Trailing 12 months
4 clearances under product code OXO in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code OXO, trailing twelve months
MonthClearances
November 20252
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260