FDA 510(k)

G CAST

K-Number: K822956 · 1982-10-26

Decision Date1982-10-26

Product CodeEJT

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

G CAST is the device name listed in this FDA 510(k) record. The listed applicant is J. Aderer, Inc.. It received FDA 510(k) clearance on 1982-10-26 under 510(k) number K822956. 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 G CAST?

G CAST is a medical device that received FDA 510(k) clearance on 1982-10-26. The listed applicant is J. Aderer, Inc.. The 510(k) number is K822956.

When did G CAST receive FDA 510(k) clearance?

G CAST received FDA 510(k) clearance on 1982-10-26, under 510(k) number K822956.

Who is the listed applicant for G CAST?

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

What is the FDA product code for G CAST?

The FDA product code for G CAST is EJT.

Other records listing J. Aderer, 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.

K822957PURCAST K82179882 ALLOY K821832DEGUCAST U K821572DUALLOR 'R'K821590PORS-ON K821407DEVA M

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Related Devices (Code: EJT)

K052463PROMETAL HN86Prometal Technologies K041378BIO 60Kodent, Inc.K040672PORTA REFLEXWieland Dental + Technik GmbH & Co. KG K040524PORTA SOLDER 1090 WWieland Dental + Technik GmbH & Co. KG K040043NDX-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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.