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FDA 510(k)

GDC-1433 A CASTING ALLOY

K-Number: K850102 · 1985-02-08

ApplicantDeringer-Ney, Inc.
Decision Date1985-02-08
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GDC-1433 A CASTING ALLOY is the device name listed in this FDA 510(k) record. The listed applicant is Deringer-Ney, Inc.. It received FDA 510(k) clearance on 1985-02-08 under 510(k) number K850102. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GDC-1433 A CASTING ALLOY?

GDC-1433 A CASTING ALLOY is a medical device that received FDA 510(k) clearance on 1985-02-08. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K850102.

When did GDC-1433 A CASTING ALLOY receive FDA 510(k) clearance?

GDC-1433 A CASTING ALLOY received FDA 510(k) clearance on 1985-02-08, under 510(k) number K850102.

Who is the listed applicant for GDC-1433 A CASTING ALLOY?

The FDA 510(k) record lists Deringer-Ney, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GDC-1433 A CASTING ALLOY?

The FDA product code for GDC-1433 A CASTING ALLOY is EJS.

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Other records listing Deringer-Ney, Inc. 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.

K933178GDC 3509K930481DENTAL CASTING ALLOY MODIFICATION-PF-4K930482DENTAL CASTING ALLOY, MODIFICATION - PF-3K925273GDC 3445K920922GDC 3367K920060DENTAL SOLDER ALLOY

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Related Devices (Code: EJS)

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.

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KGK022252STERNGOLD 1, MODEL 1127781SterngoldK022469ECO E4Wieland Dental + Technik GmbH & Co. KGK021367STERNGOLD 66, MODEL #1180230SterngoldK020195SIMIDUR S1SWieland Dental + Technik GmbH & Co. KG

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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