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FDA 510(k)

FIBIOCORE

K-Number: K020431 · 2002-07-03

ApplicantEst. Anthogyr
Decision Date2002-07-03
Product CodeELR
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIBIOCORE is the device name listed in this FDA 510(k) record. The listed applicant is Est. Anthogyr. It received FDA 510(k) clearance on 2002-07-03 under 510(k) number K020431. The device is classified under product code ELR. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBIOCORE?

FIBIOCORE is a medical device that received FDA 510(k) clearance on 2002-07-03. The listed applicant is Est. Anthogyr. The 510(k) number is K020431.

When did FIBIOCORE receive FDA 510(k) clearance?

FIBIOCORE received FDA 510(k) clearance on 2002-07-03, under 510(k) number K020431.

Who is the listed applicant for FIBIOCORE?

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

What is the FDA product code for FIBIOCORE?

The FDA product code for FIBIOCORE is ELR.

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 Est. Anthogyr 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.

K070084MONTBLANC IMPLANTOLOGY CONTRA ANGLE CONTROLK060317ANTHOGYR CONTRA ANGLES AND HANDPIECES

Related Devices (Code: ELR)

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.

K060075FIBER-METAL POSTForemost Dental, LLCK042848FRC POSTEC PLUSIvoclar Vivadent, Inc.K030820EVERSTICK POSTStick Tech , Ltd.K012496CARBON POSTJ. Morita USA, Inc.K013802FRC POSTECIvoclar Vivadent, Inc.K012849GLASS POSTJ. Morita USA, Inc.

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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