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FDA 510(k)

FIBERFILL AGP

K-Number: K023818 · 2003-04-03

ApplicantPentron Clinical Technologies
Decision Date2003-04-03
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FIBERFILL AGP is the device name listed in this FDA 510(k) record. The listed applicant is Pentron Clinical Technologies. It received FDA 510(k) clearance on 2003-04-03 under 510(k) number K023818. The device is classified under product code KIF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FIBERFILL AGP?

FIBERFILL AGP is a medical device that received FDA 510(k) clearance on 2003-04-03. The listed applicant is Pentron Clinical Technologies. The 510(k) number is K023818.

When did FIBERFILL AGP receive FDA 510(k) clearance?

FIBERFILL AGP received FDA 510(k) clearance on 2003-04-03, under 510(k) number K023818.

Who is the listed applicant for FIBERFILL AGP?

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

What is the FDA product code for FIBERFILL AGP?

The FDA product code for FIBERFILL AGP is KIF.

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Other records listing Pentron Clinical Technologies 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.

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Related Devices (Code: KIF)

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.

K262050Vioseal XSpident Co., Ltd.K253909NeoPEX™ Pre-Mixed Obturation PasteNuSmile, Ltd.K261514Calcium Hydroxide Temporary Filling Material (KP-Cal)Guilin Kevin Peter Technology Co., Ltd.K261415Injectable Root Canal Sealer (KP-Root SP)Guilin Kevin Peter Technology Co., Ltd.K253167Any-PasteMediclus Co., Ltd.K252890ZenSeal ProKerr Corporation

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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