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FDA 510(k)

HYDRON ROOT CANAL FILLING MATERIAL

K-Number: K801482 · 1980-07-21

ApplicantNational Patent Development Corp.
Decision Date1980-07-21
Product CodeKIF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

HYDRON ROOT CANAL FILLING MATERIAL is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1980-07-21 under 510(k) number K801482. 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 HYDRON ROOT CANAL FILLING MATERIAL?

HYDRON ROOT CANAL FILLING MATERIAL is a medical device that received FDA 510(k) clearance on 1980-07-21. The listed applicant is National Patent Development Corp.. The 510(k) number is K801482.

When did HYDRON ROOT CANAL FILLING MATERIAL receive FDA 510(k) clearance?

HYDRON ROOT CANAL FILLING MATERIAL received FDA 510(k) clearance on 1980-07-21, under 510(k) number K801482.

Who is the listed applicant for HYDRON ROOT CANAL FILLING MATERIAL?

The FDA 510(k) record lists National Patent Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HYDRON ROOT CANAL FILLING MATERIAL?

The FDA product code for HYDRON ROOT CANAL FILLING MATERIAL is KIF.

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Other records listing National Patent Development Corp. 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.

K843974VARIABLE TEMPERATURE CAUTERY DEVICEK832699HYDRON WOUND DRESSING FAST SEAT KITK822793PIO ROOT CANAL INDICATORK820028ZEON COMPOSITE RESIN LIGHT CURE SYSK820006ZEON COMPOSITE RESIN SYSTEMK811446HYDRON WOUND DRESSING KIT

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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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