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FDA 510(k)

DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830)

K-Number: K992896 · 1999-09-03

Decision Date1999-09-03
Product CodeEGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830) is the device name listed in this FDA 510(k) record. The listed applicant is Dental X-Ray Support Systems, Inc.. It received FDA 510(k) clearance on 1999-09-03 under 510(k) number K992896. The device is classified under product code EGY. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830)?

DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830) is a medical device that received FDA 510(k) clearance on 1999-09-03. The listed applicant is Dental X-Ray Support Systems, Inc.. The 510(k) number is K992896.

When did DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830) receive FDA 510(k) clearance?

DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830) received FDA 510(k) clearance on 1999-09-03, under 510(k) number K992896.

Who is the listed applicant for DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830)?

The FDA 510(k) record lists Dental X-Ray Support Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830)?

The FDA product code for DXSS AUTOMATIC X-RAY FILM PROCESSOR, (MODELS #S: 512, 1530, 812, 830) is EGY.

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.

Related Devices (Code: EGY)

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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