Medical Device
Manufacturing
THE TRADE PAPER OF THE FACTORY FLOOR
K912410Substantially Equivalent

Coxel Flinger 2500/5000 3-D Imaging System

Reality Imaging Corp., Solon OH / Traditional, Substantially Equivalent

K912410 is the FDA 510(k) clearance record for COXEL FLINGER 2500/5000 3-D IMAGING SYSTEM, a class II device, cleared for Reality Imaging Corp. on under FDA product code LNH (System, Nuclear Magnetic Resonance Imaging). FDA records list 2 510(k) clearances for Reality Imaging Corp., from to . As of , FDA records show no recalls naming K912410.

Clearance record

Decision date
Received
(74 days to decision)
Product code
LNH System, Nuclear Magnetic Resonance Imaging
Regulation
21 CFR 892.1000
Device class
Class II
Review panel
Radiology
Applicant
Reality Imaging Corp. 6661 Cochran Rd., Solon OH
510(k) summary
Statement
Third party review
No

Clearances, product code LNH

Trailing 12 months
26 clearances under product code LNH in the twelve months to October 2026, March 2026 the highest month at 6.
Show the numbers
Monthly 510(k) clearances under FDA product code LNH, trailing twelve months
MonthClearances
November 20251
December 20253
January 20261
February 20264
March 20266
April 20261
May 20261
June 20260
July 20262
August 20263
September 20263
October 20261