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FDA 510(k)

SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL)

K-Number: K893800 · 1989-12-20

ApplicantDeringer-Ney, Inc.
Decision Date1989-12-20
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL) is the device name listed in this FDA 510(k) record. The listed applicant is Deringer-Ney, Inc.. It received FDA 510(k) clearance on 1989-12-20 under 510(k) number K893800. 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 SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL)?

SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL) is a medical device that received FDA 510(k) clearance on 1989-12-20. The listed applicant is Deringer-Ney, Inc.. The 510(k) number is K893800.

When did SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL) receive FDA 510(k) clearance?

SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL) received FDA 510(k) clearance on 1989-12-20, under 510(k) number K893800.

Who is the listed applicant for SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL)?

The FDA 510(k) record lists Deringer-Ney, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL)?

The FDA product code for SEQUEL (CASTING ALLOY FOR PORCELAIN-FUSED-METAL) is EJT.

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Other records listing Deringer-Ney, Inc. 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.

K933178GDC 3509K930481DENTAL CASTING ALLOY MODIFICATION-PF-4K930482DENTAL CASTING ALLOY, MODIFICATION - PF-3K925273GDC 3445K920922GDC 3367K920060DENTAL SOLDER ALLOY

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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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