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)

DIGITAL RADIOGRAPHY, MODEL CXDI-55C

K-Number: K091436 · 2009-05-29

ApplicantCanon, Inc.
Decision Date2009-05-29
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DIGITAL RADIOGRAPHY, MODEL CXDI-55C is the device name listed in this FDA 510(k) record. The listed applicant is Canon, Inc.. It received FDA 510(k) clearance on 2009-05-29 under 510(k) number K091436. The device is classified under product code MQB. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL RADIOGRAPHY, MODEL CXDI-55C?

DIGITAL RADIOGRAPHY, MODEL CXDI-55C is a medical device that received FDA 510(k) clearance on 2009-05-29. The listed applicant is Canon, Inc.. The 510(k) number is K091436.

When did DIGITAL RADIOGRAPHY, MODEL CXDI-55C receive FDA 510(k) clearance?

DIGITAL RADIOGRAPHY, MODEL CXDI-55C received FDA 510(k) clearance on 2009-05-29, under 510(k) number K091436.

Who is the listed applicant for DIGITAL RADIOGRAPHY, MODEL CXDI-55C?

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

What is the FDA product code for DIGITAL RADIOGRAPHY, MODEL CXDI-55C?

The FDA product code for DIGITAL RADIOGRAPHY, MODEL CXDI-55C is MQB.

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 Canon, Inc. 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.

K252503Intelligent NRK241049CANON Fundus Camera CR-10 (CR-10)K232298DIGITAL RADIOGRAPHY CXDI-RF Wireless BlK230175Digital Radiography CXDI-CS01K222855Digital Radiography CXDI-Pro, Digital Radiography D1K222687Digital Radiography CXDI-Elite, Digital Radiography E1

View all 41 devices →

Related Devices (Code: MQB)

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.

K2538000909FCE, 0909FCE-HSRayence Co., Ltd.K260820VIVIX-S 4386W (FXRD-4386WA)Vieworks Co., Ltd.K252996Universal 1417PIKonica Minolta Healthcare Americas, Inc.K252911Lux HD 2530 detector (Lux HD 2530)Iray Imaging Technology (Haining) LimitedK250211Yushan X-Ray Flat Panel DetectorInnocare Optoelectronics Corp.K250665SKR 3000Konica Minolta, 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.

↑