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FDA 510(k)

PXS MODEL PXS7-730EA DENTAL X-RAY SOURCE

K-Number: K875212 · 1988-06-17

ApplicantKevex Corp.
Decision Date1988-06-17
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PXS MODEL PXS7-730EA DENTAL X-RAY SOURCE is the device name listed in this FDA 510(k) record. The listed applicant is Kevex Corp.. It received FDA 510(k) clearance on 1988-06-17 under 510(k) number K875212. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PXS MODEL PXS7-730EA DENTAL X-RAY SOURCE?

PXS MODEL PXS7-730EA DENTAL X-RAY SOURCE is a medical device that received FDA 510(k) clearance on 1988-06-17. The listed applicant is Kevex Corp.. The 510(k) number is K875212.

When did PXS MODEL PXS7-730EA DENTAL X-RAY SOURCE receive FDA 510(k) clearance?

PXS MODEL PXS7-730EA DENTAL X-RAY SOURCE received FDA 510(k) clearance on 1988-06-17, under 510(k) number K875212.

Who is the listed applicant for PXS MODEL PXS7-730EA DENTAL X-RAY SOURCE?

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

What is the FDA product code for PXS MODEL PXS7-730EA DENTAL X-RAY SOURCE?

The FDA product code for PXS MODEL PXS7-730EA DENTAL X-RAY SOURCE is EHD.

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Related Devices (Code: EHD)

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.

K260795Hand-held Dental X-ray System (HyperLight-M)Changzhou Sifary Medical Technology Co., Ltd.K260367Portable Dental X-ray System Model PDX novaPDX Co., Ltd.K253864NOMAD Pro 3Dental Imaging Technologies CorporationK252110Dental X-RAY Unit (AJX200)Guangzhou Ajax Medical Equipment Co., Ltd.K254018Portable Dental X-ray Device (GT-1)Guilin Refine Medical Instrument Co., Ltd.K252909Diagnostic X-Ray Equipment Model POCT22Ningbo Runyes Medical Instrument Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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