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FDA 510(k)

UPCERA ZIRCONIA BLANKS

K-Number: K093560 · 2010-01-28

ApplicantShenyang Upcera Co., Ltd.
Decision Date2010-01-28
Product CodeEIH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

UPCERA ZIRCONIA BLANKS is the device name listed in this FDA 510(k) record. The listed applicant is Shenyang Upcera Co., Ltd.. It received FDA 510(k) clearance on 2010-01-28 under 510(k) number K093560. The device is classified under product code EIH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UPCERA ZIRCONIA BLANKS?

UPCERA ZIRCONIA BLANKS is a medical device that received FDA 510(k) clearance on 2010-01-28. The listed applicant is Shenyang Upcera Co., Ltd.. The 510(k) number is K093560.

When did UPCERA ZIRCONIA BLANKS receive FDA 510(k) clearance?

UPCERA ZIRCONIA BLANKS received FDA 510(k) clearance on 2010-01-28, under 510(k) number K093560.

Who is the listed applicant for UPCERA ZIRCONIA BLANKS?

The FDA 510(k) record lists Shenyang Upcera Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UPCERA ZIRCONIA BLANKS?

The FDA product code for UPCERA ZIRCONIA BLANKS is EIH.

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Related Devices (Code: EIH)

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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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