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FDA 510(k)

STABILOR G

K-Number: K951782 · 1995-06-01

ApplicantDegussa Corp.
Decision Date1995-06-01
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STABILOR G is the device name listed in this FDA 510(k) record. The listed applicant is Degussa Corp.. It received FDA 510(k) clearance on 1995-06-01 under 510(k) number K951782. 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 STABILOR G?

STABILOR G is a medical device that received FDA 510(k) clearance on 1995-06-01. The listed applicant is Degussa Corp.. The 510(k) number is K951782.

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

STABILOR G received FDA 510(k) clearance on 1995-06-01, under 510(k) number K951782.

Who is the listed applicant for STABILOR G?

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 STABILOR G?

The FDA product code for STABILOR G is EJT.

Related Clinical Trials

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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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

View all 24 devices →

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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