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FDA 510(k)

DEGUFILL (TM) ETCHANT GEL

K-Number: K902743 · 1990-08-01

ApplicantDegussa AG
Decision Date1990-08-01
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DEGUFILL (TM) ETCHANT GEL is the device name listed in this FDA 510(k) record. The listed applicant is Degussa AG. It received FDA 510(k) clearance on 1990-08-01 under 510(k) number K902743. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEGUFILL (TM) ETCHANT GEL?

DEGUFILL (TM) ETCHANT GEL is a medical device that received FDA 510(k) clearance on 1990-08-01. The listed applicant is Degussa AG. The 510(k) number is K902743.

When did DEGUFILL (TM) ETCHANT GEL receive FDA 510(k) clearance?

DEGUFILL (TM) ETCHANT GEL received FDA 510(k) clearance on 1990-08-01, under 510(k) number K902743.

Who is the listed applicant for DEGUFILL (TM) ETCHANT GEL?

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

What is the FDA product code for DEGUFILL (TM) ETCHANT GEL?

The FDA product code for DEGUFILL (TM) ETCHANT GEL is EBF.

Related Clinical Trials

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Other records listing Degussa AG 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.

K953344DEGUBOND ULTRAK931808DUCERAGOLD, DUCERATINK926347DUCERANIUM UK922790DEGUCAST 40K921772BIOLORK921479DUCERATIN/DUCERAM LFC DENTAL PORCELAIN

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Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, Inc.

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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