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FDA 510(k)

BISCO CORE PASTE

K-Number: K921439 · 1992-05-11

ApplicantBisco, Inc.
Decision Date1992-05-11
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BISCO CORE PASTE is the device name listed in this FDA 510(k) record. The listed applicant is Bisco, Inc.. It received FDA 510(k) clearance on 1992-05-11 under 510(k) number K921439. 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 BISCO CORE PASTE?

BISCO CORE PASTE is a medical device that received FDA 510(k) clearance on 1992-05-11. The listed applicant is Bisco, Inc.. The 510(k) number is K921439.

When did BISCO CORE PASTE receive FDA 510(k) clearance?

BISCO CORE PASTE received FDA 510(k) clearance on 1992-05-11, under 510(k) number K921439.

Who is the listed applicant for BISCO CORE PASTE?

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 CORE PASTE?

The FDA product code for BISCO CORE PASTE is EBF.

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Other records listing Bisco, Inc. as applicant

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Related Devices (Code: EBF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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