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FDA 510(k)

G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER

K-Number: K880764 · 1988-04-12

ApplicantG-C Intl. Corp.
Decision Date1988-04-12
Product CodeELL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER is the device name listed in this FDA 510(k) record. The listed applicant is G-C Intl. Corp.. It received FDA 510(k) clearance on 1988-04-12 under 510(k) number K880764. The device is classified under product code ELL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER?

G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER is a medical device that received FDA 510(k) clearance on 1988-04-12. The listed applicant is G-C Intl. Corp.. The 510(k) number is K880764.

When did G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER receive FDA 510(k) clearance?

G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER received FDA 510(k) clearance on 1988-04-12, under 510(k) number K880764.

Who is the listed applicant for G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER?

The FDA 510(k) record lists G-C Intl. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER?

The FDA product code for G-CERA PORCELAIN & G-CERA PORCELAIN MODIFIER is ELL.

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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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