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FDA 510(k)

GDC-1054

K-Number: K810789 · 1981-04-14

ApplicantDeringer-Ney, Inc.
Decision Date1981-04-14
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

GDC-1054 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 1981-04-14 under 510(k) number K810789. The device is classified under product code EJT. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GDC-1054?

GDC-1054 is a medical device that received FDA 510(k) clearance on 1981-04-14. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K810789.

When did GDC-1054 receive FDA 510(k) clearance?

GDC-1054 received FDA 510(k) clearance on 1981-04-14, under 510(k) number K810789.

Who is the listed applicant for GDC-1054?

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-1054?

The FDA product code for GDC-1054 is EJT.

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.

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Related Devices (Code: EJT)

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.

K052463PROMETAL HN86Prometal TechnologiesK041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KGK040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KGK040043NDX-40 ALLOYHeraeus Kulzer, Inc.K034049HERADOR EC, PF, C, H, NH, G, GG AND MP; HERALOY U AND G; HERABOND N; ALBABOND C, B AND A; BIO HERANORMHeraeus Kulzer,GmbH

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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