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FDA 510(k)

TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P

K-Number: K024046 · 2003-02-06

ApplicantBisco, Inc.
Decision Date2003-02-06
Product CodeEBD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 2003-02-06 under 510(k) number K024046. The device is classified under product code EBD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P?

TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P is a medical device that received FDA 510(k) clearance on 2003-02-06. The listed applicant is Bisco, Inc.. The 510(k) number is K024046.

When did TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P receive FDA 510(k) clearance?

TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P received FDA 510(k) clearance on 2003-02-06, under 510(k) number K024046.

Who is the listed applicant for TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P?

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 TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P?

The FDA product code for TESCERA GLAZING RESIN, MODEL T-1804, BISCOVER XT, MODEL G-93220P is EBD.

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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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