MODEL 410 DENTAL X-RAY FILM PROCESSORS
K-Number: K874118 · 1987-11-06
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Device Summary
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
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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