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FDA 510(k)

BENNETT X-RAY TOMOGRAPHY SYSTEM

K-Number: K945749 · 1995-02-15

ApplicantBennett X-Ray Corp.
Decision Date1995-02-15
Product CodeIZF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BENNETT X-RAY TOMOGRAPHY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bennett X-Ray Corp.. It received FDA 510(k) clearance on 1995-02-15 under 510(k) number K945749. The device is classified under product code IZF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BENNETT X-RAY TOMOGRAPHY SYSTEM?

BENNETT X-RAY TOMOGRAPHY SYSTEM is a medical device that received FDA 510(k) clearance on 1995-02-15. The listed applicant is Bennett X-Ray Corp.. The 510(k) number is K945749.

When did BENNETT X-RAY TOMOGRAPHY SYSTEM receive FDA 510(k) clearance?

BENNETT X-RAY TOMOGRAPHY SYSTEM received FDA 510(k) clearance on 1995-02-15, under 510(k) number K945749.

Who is the listed applicant for BENNETT X-RAY TOMOGRAPHY SYSTEM?

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

What is the FDA product code for BENNETT X-RAY TOMOGRAPHY SYSTEM?

The FDA product code for BENNETT X-RAY TOMOGRAPHY SYSTEM is IZF.

Related Clinical Trials

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Other records listing Bennett X-Ray 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.

K964576PROFILE MAMMOGRAPHY SYSTEM (M-PRO)K952672VERTICAL INTEGRATED PERFECT VIEW (VIP) RADIOGRAPHIC SYSTEMK944978BENNETT X-RAY DIGITAL SPOT IMAGING SYSTEM MODEL M-DSIK945962BENNETT X-RAY PROFILE POSITIONING PADDLE FOR MAMMOGRAPHYK945731HFQ HIGH FREQUENCY RADIOGRAPHIC AND FLUROSCOPIC GENERATORSK940701BENNETT MAMMOGRAPHY POSITIONING CHAIR MODEL NO. M-PCH

View all 23 devices →

Related Devices (Code: IZF)

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.

K252649TAP2DNano-X Imaging , Ltd.K252133Adaptix Ortho350Adaptix LimitedK250850Nanox.ARC XNano-X Imaging , Ltd.K242395Nanox.ARCNano-X Imaging , Ltd.K222934Nanox.ARCNano-X Imaging , Ltd.K221949Ortho Device, ADAPTIX 3D Orthopedic Imaging SystemPausch Medical 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.

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