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FDA 510(k)

MODEL 410 DENTAL X-RAY FILM PROCESSORS

K-Number: K874118 · 1987-11-06

ApplicantDent-X Co.
Decision Date1987-11-06
Product CodeEGY
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 410 DENTAL X-RAY FILM PROCESSORS is the device name listed in this FDA 510(k) record. The listed applicant is Dent-X Co.. It received FDA 510(k) clearance on 1987-11-06 under 510(k) number K874118. 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 MODEL 410 DENTAL X-RAY FILM PROCESSORS?

MODEL 410 DENTAL X-RAY FILM PROCESSORS is a medical device that received FDA 510(k) clearance on 1987-11-06. The listed applicant is Dent-X Co.. The 510(k) number is K874118.

When did MODEL 410 DENTAL X-RAY FILM PROCESSORS receive FDA 510(k) clearance?

MODEL 410 DENTAL X-RAY FILM PROCESSORS received FDA 510(k) clearance on 1987-11-06, under 510(k) number K874118.

Who is the listed applicant for MODEL 410 DENTAL X-RAY FILM PROCESSORS?

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

What is the FDA product code for MODEL 410 DENTAL X-RAY FILM PROCESSORS?

The FDA product code for MODEL 410 DENTAL X-RAY FILM PROCESSORS 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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