RAD SOURCE X-RAY BLOOD IRRADIATOR, MODEL RS-3400— 510(k) K082921

Name: FDA 510(k) clearance K082921
Creator: U.S. Food and Drug Administration
Published: 2009-02-17

Substantially Equivalent

Rad Source Technologies, Inc.

FDA 510(k) clearance K082921 for RAD SOURCE X-RAY BLOOD IRRADIATOR, MODEL RS-3400, Substantially Equivalent on 2009-02-17. Applicant: Rad Source Technologies, Inc.. Device class: Unclassified.

Clearance details

Applicant: Rad Source Technologies, Inc.
Product code: Code MOT
Device class: Unclassified
Advisory panel: Unknown
Date received: 2008-10-01
Decision date: 2009-02-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Alpharetta, GA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code MOT

view all

K201177 — RadGil22020-08-17
K181737 — Raycell MK12019-01-02
K172087 — SANGRAY2017-10-27
K161324 — Raycell Mk22016-08-12
K051065 — RAYCELL X-RAY BLOOD IRRADIATOR2005-05-26

Data sourced from openFDA. This site is unofficial and independent of the FDA.