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FDA 510(k)

PLATINLLOYD 100

K-Number: K983079 · 1998-10-23

ApplicantBego U.S.A.
Decision Date1998-10-23
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PLATINLLOYD 100 is the device name listed in this FDA 510(k) record. The listed applicant is Bego U.S.A.. It received FDA 510(k) clearance on 1998-10-23 under 510(k) number K983079. 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 PLATINLLOYD 100?

PLATINLLOYD 100 is a medical device that received FDA 510(k) clearance on 1998-10-23. The listed applicant is Bego U.S.A.. The 510(k) number is K983079.

When did PLATINLLOYD 100 receive FDA 510(k) clearance?

PLATINLLOYD 100 received FDA 510(k) clearance on 1998-10-23, under 510(k) number K983079.

Who is the listed applicant for PLATINLLOYD 100?

The FDA 510(k) record lists Bego U.S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLATINLLOYD 100?

The FDA product code for PLATINLLOYD 100 is EJT.

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Other records listing Bego U.S.A. 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.

K033279GOLD DENTAL CASTING ALLOYSK032136WIROBOND CK983080AUROLLOYD KFK983082BEGOCER GK983078BEGOPALK983077BIO PONTOSTAR

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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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