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FDA 510(k)

CASTA-LLOY

K-Number: K800951 · 1980-05-08

ApplicantU.S. Shizai Corp.
Decision Date1980-05-08
Product CodeEJS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CASTA-LLOY is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Shizai Corp.. It received FDA 510(k) clearance on 1980-05-08 under 510(k) number K800951. 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 CASTA-LLOY?

CASTA-LLOY is a medical device that received FDA 510(k) clearance on 1980-05-08. The listed applicant is U.S. Shizai Corp.. The 510(k) number is K800951.

When did CASTA-LLOY receive FDA 510(k) clearance?

CASTA-LLOY received FDA 510(k) clearance on 1980-05-08, under 510(k) number K800951.

Who is the listed applicant for CASTA-LLOY?

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

What is the FDA product code for CASTA-LLOY?

The FDA product code for CASTA-LLOY is EJS.

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Other records listing U.S. Shizai Corp. 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.

K853841HARMO SONICK822464OBTURATION GUTTAK820639OBTURATION SYSTEM KITK802189DENTLOID

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

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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