F-G-P TRAY
K-Number: K842274 · 1984-07-31
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Device Summary
Frequently Asked Questions
What is the F-G-P TRAY?
F-G-P TRAY is a medical device that received FDA 510(k) clearance on 1984-07-31. The listed applicant is Di-Equi Dental Products. The 510(k) number is K842274.
When did F-G-P TRAY receive FDA 510(k) clearance?
F-G-P TRAY received FDA 510(k) clearance on 1984-07-31, under 510(k) number K842274.
Who is the listed applicant for F-G-P TRAY?
The FDA 510(k) record lists Di-Equi Dental Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for F-G-P TRAY?
The FDA product code for F-G-P TRAY is EHY.
Other records listing Di-Equi Dental Products 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.
Related Devices (Code: EHY)
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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