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FDA 510(k)

DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL

K-Number: K920560 · 1992-03-02

ApplicantInvoclar North America, Inc.
Decision Date1992-03-02
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL is the device name listed in this FDA 510(k) record. The listed applicant is Invoclar North America, Inc.. It received FDA 510(k) clearance on 1992-03-02 under 510(k) number K920560. The device is classified under product code EJS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL?

DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL is a medical device that received FDA 510(k) clearance on 1992-03-02. The listed applicant is Invoclar North America, Inc.. The 510(k) number is K920560.

When did DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL receive FDA 510(k) clearance?

DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL received FDA 510(k) clearance on 1992-03-02, under 510(k) number K920560.

Who is the listed applicant for DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL?

The FDA 510(k) record lists Invoclar North America, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL?

The FDA product code for DW236-34 ALLOY FOR PORCELAIN FUSED TO METAL is EJS.

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 Invoclar North America, 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.

K932774DW232 #31

Related Devices (Code: EJS)

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.

K041433BRIGHT GOLD XHIvoclar Vivadent, Inc.K040436SIMIDUR SUPERIORWieland Dental + Technik GmbH & Co. KGK022252STERNGOLD 1, MODEL 1127781SterngoldK022469ECO E4Wieland Dental + Technik GmbH & Co. KGK021367STERNGOLD 66, MODEL #1180230SterngoldK020195SIMIDUR S1SWieland Dental + Technik GmbH & Co. KG

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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