510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K834281Substantially Equivalent

Rad II Simulator

Haynes Radiation Ltd., Inc., Alameda CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K834281 is the FDA 510(k) clearance record for RAD II SIMULATOR, a class II device, cleared for Haynes Radiation Ltd., Inc. on under FDA product code KPQ (System, Simulation, Radiation Therapy). FDA records list 2 510(k) clearances for Haynes Radiation Ltd., Inc., from to . As of , FDA records show no recalls naming K834281.

Clearance record

Decision date
Received
(57 days to decision)
Product code
KPQ System, Simulation, Radiation Therapy
Regulation
21 CFR 892.5840
Device class
Class II
Review panel
Radiology
Applicant
Haynes Radiation Ltd., Inc. P.O. Box 1312, Alameda CA
Third party review
No

Clearances, product code KPQ

Trailing 12 months

FDA records hold no clearances under product code KPQ in the trailing twelve months.

FDA records show no clearances under product code KPQ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KPQ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260