510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K862120Substantially Equivalent

Scx System

General Electric Co., Milwaukee WI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K862120 is the FDA 510(k) clearance record for SCX SYSTEM, a class II device, cleared for General Electric Co. on under FDA product code JAA (System, X-Ray, Fluoroscopic, Image-Intensified). FDA records list 256 510(k) clearances for General Electric Co., from to . As of , FDA records show 3 recalls naming K862120.

Clearance record

Decision date
Received
(13 days to decision)
Product code
JAA System, X-Ray, Fluoroscopic, Image-Intensified
Regulation
21 CFR 892.1650
Device class
Class II
Review panel
Radiology
Applicant
General Electric Co. P.O. Box 414, Milwaukee WI
Third party review
No

Clearances, product code JAA

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