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)

VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS

K-Number: K071193 · 2007-05-30

ApplicantVidar Systems Corp.
Decision Date2007-05-30
Product CodeMQB
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Vidar Systems Corp.. It received FDA 510(k) clearance on 2007-05-30 under 510(k) number K071193. 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 VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS?

VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS is a medical device that received FDA 510(k) clearance on 2007-05-30. The listed applicant is Vidar Systems Corp.. The 510(k) number is K071193.

When did VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS receive FDA 510(k) clearance?

VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS received FDA 510(k) clearance on 2007-05-30, under 510(k) number K071193.

Who is the listed applicant for VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS?

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

What is the FDA product code for VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS?

The FDA product code for VIDAR VISION 3000 AND 4000 X-RAY SYSTEMS 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 Vidar Systems 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.

K130636TELERADPRO EDGE; TELERADPRO EDGE HD-CCDK130406DIAGNOSTICPRO EDGEK102476TELERADPROK093809VIDAR DENTAL FILM DIGITIZERK070563VIDAR VISION 2000K024171VIDAR BONE TRACK SYSTEM SOFTWARE

View all 13 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.

↑