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FDA 510(k)

FUJI LINING CEMENT LIGHT CURE

K-Number: K901999 · 1990-07-31

ApplicantG-C Intl. Corp.
Decision Date1990-07-31
Product CodeEJK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FUJI LINING CEMENT LIGHT CURE 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 1990-07-31 under 510(k) number K901999. The device is classified under product code EJK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FUJI LINING CEMENT LIGHT CURE?

FUJI LINING CEMENT LIGHT CURE is a medical device that received FDA 510(k) clearance on 1990-07-31. The listed applicant is G-C Intl. Corp.. The 510(k) number is K901999.

When did FUJI LINING CEMENT LIGHT CURE receive FDA 510(k) clearance?

FUJI LINING CEMENT LIGHT CURE received FDA 510(k) clearance on 1990-07-31, under 510(k) number K901999.

Who is the listed applicant for FUJI LINING CEMENT LIGHT CURE?

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 FUJI LINING CEMENT LIGHT CURE?

The FDA product code for FUJI LINING CEMENT LIGHT CURE is EJK.

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Other records listing G-C Intl. Corp. as applicant

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Related Devices (Code: EJK)

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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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