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FDA 510(k)

UNIVERSAL CERAMIC SOLDER

K-Number: K022969 · 2002-10-18

ApplicantIvoclar Vivadent, Inc.
Decision Date2002-10-18
Product CodeEJT
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UNIVERSAL CERAMIC SOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar Vivadent, Inc.. It received FDA 510(k) clearance on 2002-10-18 under 510(k) number K022969. 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 UNIVERSAL CERAMIC SOLDER?

UNIVERSAL CERAMIC SOLDER is a medical device that received FDA 510(k) clearance on 2002-10-18. The listed applicant is Ivoclar Vivadent, Inc.. The 510(k) number is K022969.

When did UNIVERSAL CERAMIC SOLDER receive FDA 510(k) clearance?

UNIVERSAL CERAMIC SOLDER received FDA 510(k) clearance on 2002-10-18, under 510(k) number K022969.

Who is the listed applicant for UNIVERSAL CERAMIC SOLDER?

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

What is the FDA product code for UNIVERSAL CERAMIC SOLDER?

The FDA product code for UNIVERSAL CERAMIC SOLDER is EJT.

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Related Devices (Code: EJT)

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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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