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FDA 510(k)

CERALOY

K-Number: K021971 · 2002-08-01

ApplicantNeirynck & Vogt NV
Decision Date2002-08-01
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERALOY is the device name listed in this FDA 510(k) record. The listed applicant is Neirynck & Vogt NV. It received FDA 510(k) clearance on 2002-08-01 under 510(k) number K021971. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CERALOY?

CERALOY is a medical device that received FDA 510(k) clearance on 2002-08-01. The listed applicant is Neirynck & Vogt NV. The 510(k) number is K021971.

When did CERALOY receive FDA 510(k) clearance?

CERALOY received FDA 510(k) clearance on 2002-08-01, under 510(k) number K021971.

Who is the listed applicant for CERALOY?

The FDA 510(k) record lists Neirynck & Vogt NV as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CERALOY?

The FDA product code for CERALOY is EJH.

Related Clinical Trials

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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Other records listing Neirynck & Vogt NV 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.

K023477BIOLOYK021969CHROLOYK021968CERALOY SOLDERK021965CHROLOY SOLDER

Related Devices (Code: EJH)

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.

K123929BEGOPAL+Bego Bremer Goldschlaegerei Wilh. Herbst GmbH & COK040180CONTINUM VAalba Dent, Inc.K040179CONTINUMAalba Dent, Inc.K033356VERASOFT ESAalba Dent, Inc.K033045DREAM BOND, DREAMCAST CHROME, DREAMCAST V, DREAM FLEXICAST, DREAM LITHECASTAmerican Green Dent. Mfg, Inc.K032136WIROBOND CBego U.S.A.

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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