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FDA 510(k)

PART 872 DEGUFILL H & DEGUFILL M DA

K-Number: K914368 · 1991-11-13

ApplicantDegussa AG
Decision Date1991-11-13
Product CodeEKJ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PART 872 DEGUFILL H & DEGUFILL M DA is the device name listed in this FDA 510(k) record. The listed applicant is Degussa AG. It received FDA 510(k) clearance on 1991-11-13 under 510(k) number K914368. The device is classified under product code EKJ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PART 872 DEGUFILL H & DEGUFILL M DA?

PART 872 DEGUFILL H & DEGUFILL M DA is a medical device that received FDA 510(k) clearance on 1991-11-13. The listed applicant is Degussa AG. The 510(k) number is K914368.

When did PART 872 DEGUFILL H & DEGUFILL M DA receive FDA 510(k) clearance?

PART 872 DEGUFILL H & DEGUFILL M DA received FDA 510(k) clearance on 1991-11-13, under 510(k) number K914368.

Who is the listed applicant for PART 872 DEGUFILL H & DEGUFILL M DA?

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 PART 872 DEGUFILL H & DEGUFILL M DA?

The FDA product code for PART 872 DEGUFILL H & DEGUFILL M DA is EKJ.

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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: EKJ)

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.

K961714ASEPTYLUM, UNI-CARRIERDistriflor S.A.K953707MEDTROL DENTAL KITMedtrol, Inc.K945815DENTAL KITConstancy Ent., Inc.K951607SUREFLEX FILESDentsply Intl.K945077INSTRUMENT,FILLING,PLASTIC,DENTALWorldwide Dental, Inc.K943820STAT PAKMagnum Instruments, 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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