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FDA 510(k)

PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST

K-Number: K875313 · 1988-03-10

ApplicantBisco, Inc.
Decision Date1988-03-10
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 1988-03-10 under 510(k) number K875313. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST?

PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST is a medical device that received FDA 510(k) clearance on 1988-03-10. The listed applicant is Bisco, Inc.. The 510(k) number is K875313.

When did PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST receive FDA 510(k) clearance?

PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST received FDA 510(k) clearance on 1988-03-10, under 510(k) number K875313.

Who is the listed applicant for PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST?

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

What is the FDA product code for PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST?

The FDA product code for PORCELAIN VENEER RESIN CEMENT W/DUAL CURE CATALYST is EBF.

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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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