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FDA 510(k)

GXP DENTAL X-RAY PROCESSOR

K-Number: K932675 · 1993-07-26

ApplicantGendex Corp.
Decision Date1993-07-26
Product CodeEGN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GXP DENTAL X-RAY PROCESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Gendex Corp.. It received FDA 510(k) clearance on 1993-07-26 under 510(k) number K932675. The device is classified under product code EGN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GXP DENTAL X-RAY PROCESSOR?

GXP DENTAL X-RAY PROCESSOR is a medical device that received FDA 510(k) clearance on 1993-07-26. The listed applicant is Gendex Corp.. The 510(k) number is K932675.

When did GXP DENTAL X-RAY PROCESSOR receive FDA 510(k) clearance?

GXP DENTAL X-RAY PROCESSOR received FDA 510(k) clearance on 1993-07-26, under 510(k) number K932675.

Who is the listed applicant for GXP DENTAL X-RAY PROCESSOR?

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

What is the FDA product code for GXP DENTAL X-RAY PROCESSOR?

The FDA product code for GXP DENTAL X-RAY PROCESSOR is EGN.

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.

Other records listing Gendex 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.

View all 14 devices →

Related Devices (Code: EGN)

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.

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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