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FDA 510(k)

BENNETT X-RAY ID PLUS

K-Number: K925332 · 1992-11-27

ApplicantBennett X-Ray Technologies
Decision Date1992-11-27
Product CodeJAC
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BENNETT X-RAY ID PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Bennett X-Ray Technologies. It received FDA 510(k) clearance on 1992-11-27 under 510(k) number K925332. The device is classified under product code JAC. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BENNETT X-RAY ID PLUS?

BENNETT X-RAY ID PLUS is a medical device that received FDA 510(k) clearance on 1992-11-27. The listed applicant is Bennett X-Ray Technologies. The 510(k) number is K925332.

When did BENNETT X-RAY ID PLUS receive FDA 510(k) clearance?

BENNETT X-RAY ID PLUS received FDA 510(k) clearance on 1992-11-27, under 510(k) number K925332.

Who is the listed applicant for BENNETT X-RAY ID PLUS?

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

What is the FDA product code for BENNETT X-RAY ID PLUS?

The FDA product code for BENNETT X-RAY ID PLUS is JAC.

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 Bennett X-Ray Technologies 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.

K935428BENNETT X-RAY DIGITAL SPOT IMAGER

Related Devices (Code: JAC)

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.

K942883DIGITAL I.D. CAMERAMiles Inc., Agfa DivisionK930752CT/MRI TOPOGRAPHIC MARKERI.Z.I. Corp.K932357FUJI EC ID CAMERAFujifilm Medical System U.S.A., Inc.K925892SOLSTICE XRAY RING MARKER PADSolstice Corp.K926404KODAK X-OMATIC IDENTIFICATION CAMERA, MODEL 4 & 4LEastman Kodak CompanyK923533ADMARKPlanmeca USA, 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.

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