510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K073059Substantially Equivalent

Probeat with Discrete Spot Scanning System

Hitachi, Ltd., Power Systems Group, Washington DC / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K073059 is the FDA 510(k) clearance record for PROBEAT WITH DISCRETE SPOT SCANNING SYSTEM, a class II device, cleared for Hitachi, Ltd., Power Systems Group on under FDA product code LHN (System, Radiation Therapy, Charged-Particle, Medical). FDA records list 2 510(k) clearances for Hitachi, Ltd., Power Systems Group, from to . As of , FDA records show one recall naming K073059.

Clearance record

Decision date
Received
(41 days to decision)
Product code
LHN System, Radiation Therapy, Charged-Particle, Medical
Regulation
21 CFR 892.5050
Device class
Class II
Review panel
Radiology
Applicant
Hitachi, Ltd., Power Systems Group 555 Thirteenth St., NW, Washington DC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LHN

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