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FDA 510(k)

CERALOY SOLDER

K-Number: K021968 · 2002-07-26

ApplicantNeirynck & Vogt NV
Decision Date2002-07-26
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CERALOY SOLDER 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 2002-07-26 under 510(k) number K021968. 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 SOLDER?

CERALOY SOLDER is a medical device that received FDA 510(k) clearance on 2002-07-26. The listed applicant is Neirynck & Vogt NV. The 510(k) number is K021968.

When did CERALOY SOLDER receive FDA 510(k) clearance?

CERALOY SOLDER received FDA 510(k) clearance on 2002-07-26, under 510(k) number K021968.

Who is the listed applicant for CERALOY SOLDER?

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 SOLDER?

The FDA product code for CERALOY SOLDER 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.

K023477BIOLOYK021971CERALOYK021969CHROLOYK021965CHROLOY 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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