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FDA 510(k)

CERAMIBOND

K-Number: K802899 · 1980-12-19

ApplicantZulauf, Inc.
Decision Date1980-12-19
Product CodeDYW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERAMIBOND is the device name listed in this FDA 510(k) record. The listed applicant is Zulauf, Inc.. It received FDA 510(k) clearance on 1980-12-19 under 510(k) number K802899. The device is classified under product code DYW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERAMIBOND?

CERAMIBOND is a medical device that received FDA 510(k) clearance on 1980-12-19. The listed applicant is Zulauf, Inc.. The 510(k) number is K802899.

When did CERAMIBOND receive FDA 510(k) clearance?

CERAMIBOND received FDA 510(k) clearance on 1980-12-19, under 510(k) number K802899.

Who is the listed applicant for CERAMIBOND?

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

What is the FDA product code for CERAMIBOND?

The FDA product code for CERAMIBOND is DYW.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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