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FDA 510(k)

DEGUSTAR GA-2

K-Number: K951777 · 1995-05-31

ApplicantDegussa Corp.
Decision Date1995-05-31
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DEGUSTAR GA-2 is the device name listed in this FDA 510(k) record. The listed applicant is Degussa Corp.. It received FDA 510(k) clearance on 1995-05-31 under 510(k) number K951777. 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 DEGUSTAR GA-2?

DEGUSTAR GA-2 is a medical device that received FDA 510(k) clearance on 1995-05-31. The listed applicant is Degussa Corp.. The 510(k) number is K951777.

When did DEGUSTAR GA-2 receive FDA 510(k) clearance?

DEGUSTAR GA-2 received FDA 510(k) clearance on 1995-05-31, under 510(k) number K951777.

Who is the listed applicant for DEGUSTAR GA-2?

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 DEGUSTAR GA-2?

The FDA product code for DEGUSTAR GA-2 is EJT.

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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 HNK972910PORS ON LITEK960256DEGUDENT LSK960226DG 88K960104BIOCCLUS 4K955465DEGUPRINT

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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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