FDA 510(k)

GDC 934

K-Number: K801277 · 1980-07-21

Decision Date1980-07-21

Product CodeEJS

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

GDC 934 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 1980-07-21 under 510(k) number K801277. 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 934?

GDC 934 is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K801277.

When did GDC 934 receive FDA 510(k) clearance?

GDC 934 received FDA 510(k) clearance on 1980-07-21, under 510(k) number K801277.

Who is the listed applicant for GDC 934?

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 934?

The FDA product code for GDC 934 is EJS.

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

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Related Devices (Code: EJS)

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KG K022252STERNGOLD 1, MODEL 1127781Sterngold K022469ECO E4Wieland Dental + Technik GmbH & Co. KG K021367STERNGOLD 66, MODEL #1180230Sterngold K020195SIMIDUR 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.