FDA 510(k)

ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300

K-Number: K962140 · 1996-07-25

Decision Date1996-07-25

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300 is the device name listed in this FDA 510(k) record. The listed applicant is Continental X-Ray Corp.. It received FDA 510(k) clearance on 1996-07-25 under 510(k) number K962140. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300?

ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300 is a medical device that received FDA 510(k) clearance on 1996-07-25. The listed applicant is Continental X-Ray Corp.. The 510(k) number is K962140.

When did ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300 receive FDA 510(k) clearance?

ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300 received FDA 510(k) clearance on 1996-07-25, under 510(k) number K962140.

Who is the listed applicant for ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300?

The FDA 510(k) record lists Continental X-Ray Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300?

The FDA product code for ICT-2000, INTEGRATED C-ARM/TABLE MULTIPURPOSE RADIOGRAPHIC/FLUOROSCOPIC POSITIONING SYSTEM MODEL NO. 6896.300 is JAA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Continental X-Ray Corp. as applicant

K972442CEILING MOUNTED LATERAL POSITIONER, MODEL NO. 6896.002 K961690CARDIOARC SERIES: POSITIONER C-ARM MODELS NO. 6896.001 AND 6896.105 K954581ARC SERIES K950571LINEAR FR TOMOGRAPHIC SYSTEM: 0MT 8000, MODEL NO. 6681.270 K942175LINEAR TOMOGRAPHIC SYSTEM: PMT 6000 K942100MODEL TM EP HIGH VOLTAGE GENERATOR

View all 27 devices →

Related Devices (Code: JAA)

K253103Nexus DRF Digital X-ray Imaging SystemVarex Imaging Corporation K251650Insight Enhanced™ DRF (EN-1002-01)Imaging Engineering, LLC K242488Soteria E-ViewOmega Medical Imaging, LLC K242948Adora DRFi (04550010)Nrt X-Ray A/S K233380TRIDENT Mobile Fluoroscopy SystemDornier Medtech America K233945ProxiDiagnost N90 / Precision CRF (706110, 706400)Philips Medical Systems Dmc GmbH

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.