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FDA 510(k)

CAVIT-W

K-Number: K875133 · 1988-03-01

ApplicantEspe GmbH (Us)
Decision Date1988-03-01
Product CodeEBG
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CAVIT-W is the device name listed in this FDA 510(k) record. The listed applicant is Espe GmbH (Us). It received FDA 510(k) clearance on 1988-03-01 under 510(k) number K875133. The device is classified under product code EBG. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAVIT-W?

CAVIT-W is a medical device that received FDA 510(k) clearance on 1988-03-01. The listed applicant is Espe GmbH (Us). The 510(k) number is K875133.

When did CAVIT-W receive FDA 510(k) clearance?

CAVIT-W received FDA 510(k) clearance on 1988-03-01, under 510(k) number K875133.

Who is the listed applicant for CAVIT-W?

The FDA 510(k) record lists Espe GmbH (Us) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAVIT-W?

The FDA product code for CAVIT-W is EBG.

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Other records listing Espe GmbH (Us) as applicant

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.

K925027PHOTAC-FIL APLICAPK915005PHOTAC-BOND APLICAP, MODIFICATIONK913966SONO(R) -CEMK913857ROCATEC(R) -PLUSK913965ESPE(R) -SILK905604VISIO-GEM ART-SYSTEM

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Related Devices (Code: EBG)

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.

K261261Dura-ArchHangzhou SHINING3D Dental Technology Co., Ltd.K253380“FLNT Base” and “FLNT Temp”Liaoning Upcera Co., Ltd.K251271TempFIT Temporary Crown and Bridge ResinRizhao Huge Biomaterials Company, Ltd.K243370DentaTOOTHAsiga Pty, Ltd.K243621Evoblock, PerléonEvoden Indústria Comércio Importação E ExportaçãoK243951TEMP MASTER, PMMA-based dental resinTaiwan Dental Materials Co., Ltd.

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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