FDA 510(k)

DG 88

K-Number: K960226 · 1996-02-14

Decision Date1996-02-14

Product CodeEJT

Advisory CommitteeDE

DecisionSubstantially Equivalent

Device Summary

DG 88 is the device name listed in this FDA 510(k) record. The listed applicant is Degussa Corp.. It received FDA 510(k) clearance on 1996-02-14 under 510(k) number K960226. 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 DG 88?

DG 88 is a medical device that received FDA 510(k) clearance on 1996-02-14. The listed applicant is Degussa Corp.. The 510(k) number is K960226.

When did DG 88 receive FDA 510(k) clearance?

DG 88 received FDA 510(k) clearance on 1996-02-14, under 510(k) number K960226.

Who is the listed applicant for DG 88?

The FDA 510(k) record lists Degussa Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DG 88?

The FDA product code for DG 88 is EJT.

Other records listing Degussa Corp. 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.

K973288STABILOR HN K972910PORS ON LITE K960256DEGUDENT LS K960104BIOCCLUS 4 K955465DEGUPRINT K955118DEGUBOND X-LITE PLUS

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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.