Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

KOORDINAT ANGIO

K-Number: K781992 · 1978-12-07

ApplicantSiemens Corp.
Decision Date1978-12-07
Product CodeKXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

KOORDINAT ANGIO is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Corp.. It received FDA 510(k) clearance on 1978-12-07 under 510(k) number K781992. The device is classified under product code KXJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KOORDINAT ANGIO?

KOORDINAT ANGIO is a medical device that received FDA 510(k) clearance on 1978-12-07. The listed applicant is Siemens Corp.. The 510(k) number is K781992.

When did KOORDINAT ANGIO receive FDA 510(k) clearance?

KOORDINAT ANGIO received FDA 510(k) clearance on 1978-12-07, under 510(k) number K781992.

Who is the listed applicant for KOORDINAT ANGIO?

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

What is the FDA product code for KOORDINAT ANGIO?

The FDA product code for KOORDINAT ANGIO is KXJ.

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_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Siemens Corp. as applicant

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.

K103360DIMENSION VISTA DIGITOXIN CALIBRATOR - DGTX CALK993947KOORDINANT ANGIOGRAPHIC AND OPERATING ROOM MODEL X-RAY TABLE FAMILYK992925AX WORKSTATION DR-VIEWER SOFTWARE OPTIONK991652HIGH ENDS GRADIENTS/MAGNETOM SYMPHONY SYSTEMK991600SOMATOM PLUS 4 WITH SLIDING GANTRY OPTIONK984221FUNCTIONAL MRI PACKAGE FOR MAGETETOM VISION MR

View all 66 devices →

Related Devices (Code: KXJ)

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.

K050190APOLLOVilla Sistemi Medicali S.P.A.K963905RADIOGRAPHIC ITT TABLEX-Ray Technologies, Inc.K955414XRT 400Wuestec Medical, Inc.K951146IMAGING TABLESepta Corp.K950068CARBON FIBER COUCH INSERTMedtec, Inc.K950442INFRARED EXPOSURE HAND SWITCHMedical X-Ray Intl., Inc.

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.

↑