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FDA 510(k)

BISCO PORCELAIN REPAIR KIT

K-Number: K874557 · 1988-01-28

ApplicantBisco, Inc.
Decision Date1988-01-28
Product CodeEBC
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BISCO PORCELAIN REPAIR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 1988-01-28 under 510(k) number K874557. The device is classified under product code EBC. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BISCO PORCELAIN REPAIR KIT?

BISCO PORCELAIN REPAIR KIT is a medical device that received FDA 510(k) clearance on 1988-01-28. The listed applicant is Bisco, Inc.. The 510(k) number is K874557.

When did BISCO PORCELAIN REPAIR KIT receive FDA 510(k) clearance?

BISCO PORCELAIN REPAIR KIT received FDA 510(k) clearance on 1988-01-28, under 510(k) number K874557.

Who is the listed applicant for BISCO PORCELAIN REPAIR KIT?

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 BISCO PORCELAIN REPAIR KIT?

The FDA product code for BISCO PORCELAIN REPAIR KIT is EBC.

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Other records listing Bisco, Inc. as applicant

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Related Devices (Code: EBC)

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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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