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FDA 510(k)

MICROBOND COMPOSITE KIT FOR CERAMIC BONDING SYSTEM

K-Number: K870628 · 1987-03-06

ApplicantChem-E-Dent
Decision Date1987-03-06
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MICROBOND COMPOSITE KIT FOR CERAMIC BONDING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Chem-E-Dent. It received FDA 510(k) clearance on 1987-03-06 under 510(k) number K870628. 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 MICROBOND COMPOSITE KIT FOR CERAMIC BONDING SYSTEM?

MICROBOND COMPOSITE KIT FOR CERAMIC BONDING SYSTEM is a medical device that received FDA 510(k) clearance on 1987-03-06. The listed applicant is Chem-E-Dent. The 510(k) number is K870628.

When did MICROBOND COMPOSITE KIT FOR CERAMIC BONDING SYSTEM receive FDA 510(k) clearance?

MICROBOND COMPOSITE KIT FOR CERAMIC BONDING SYSTEM received FDA 510(k) clearance on 1987-03-06, under 510(k) number K870628.

Who is the listed applicant for MICROBOND COMPOSITE KIT FOR CERAMIC BONDING SYSTEM?

The FDA 510(k) record lists Chem-E-Dent as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROBOND COMPOSITE KIT FOR CERAMIC BONDING SYSTEM?

The FDA product code for MICROBOND COMPOSITE KIT FOR CERAMIC BONDING SYSTEM is EBF.

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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

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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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