CTPORT CT SIMULATION SYSTEM FOR RADIOTHERAPY— 510(k) K945838

Name: FDA 510(k) clearance K945838
Creator: U.S. Food and Drug Administration
Published: 1995-10-25

Substantially Equivalent

Toshiba America Medical Systems, In.C

FDA 510(k) clearance K945838 for CTPORT CT SIMULATION SYSTEM FOR RADIOTHERAPY, Substantially Equivalent on 1995-10-25. Applicant: Toshiba America Medical Systems, In.C. Device class: 2.

Clearance details

Applicant: Toshiba America Medical Systems, In.C
Product code: Code KPQ
Device class: Class 2
Regulation: 21 CFR 892.5840
Advisory panel: Radiology
Date received: 1994-11-29
Decision date: 1995-10-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tustin, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPQ

view all

K132944 — ADVANTAGESIM MD MR PELVIC ORGAN AT RISK SEGMENTATION2014-03-14
K132045 — ADVANTAGESIM MD WITH CT ATLAS-BASED CONTOURING AND RE-PLANNING OPTIONS2013-09-04
K101038 — RAD II SIMULATOR, RAD II KV IMAGER, DUAL RAD II KV IMAGER2010-08-17
K090706 — ONCENTRA SIMULATION 2.32009-06-15
K083591 — IKOENGELO, VERSION 22008-12-29

More clearances from Toshiba America Medical Systems, In.C

view all

K141472 — VANTAGE ELAN2014-09-19
K133553 — KALARE2014-06-13
K140729 — APLIO ARTIDA, V3.22014-05-23
K132106 — INFINIX ANGIO WORKSTATION W/DTS SOFTWARE2013-11-12
K131822 — ULTRAEXTEND USWS-900A V2.1 AND V3.12013-07-23

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