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FDA 510(k)

ZEON COMPOSITE RESIN LIGHT CURE SYS

K-Number: K820028 · 1982-03-11

ApplicantNational Patent Development Corp.
Decision Date1982-03-11
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ZEON COMPOSITE RESIN LIGHT CURE SYS 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 1982-03-11 under 510(k) number K820028. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEON COMPOSITE RESIN LIGHT CURE SYS?

ZEON COMPOSITE RESIN LIGHT CURE SYS is a medical device that received FDA 510(k) clearance on 1982-03-11. The listed applicant is National Patent Development Corp.. The 510(k) number is K820028.

When did ZEON COMPOSITE RESIN LIGHT CURE SYS receive FDA 510(k) clearance?

ZEON COMPOSITE RESIN LIGHT CURE SYS received FDA 510(k) clearance on 1982-03-11, under 510(k) number K820028.

Who is the listed applicant for ZEON COMPOSITE RESIN LIGHT CURE SYS?

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 ZEON COMPOSITE RESIN LIGHT CURE SYS?

The FDA product code for ZEON COMPOSITE RESIN LIGHT CURE SYS is EBF.

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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 INDICATORK820006ZEON COMPOSITE RESIN SYSTEMK811446HYDRON WOUND DRESSING KITK801482HYDRON ROOT CANAL FILLING MATERIAL

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Related Devices (Code: EBF)

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.

K262982Core·it DualSpident Co., Ltd.K262202Cerasmart ForteGC America, Inc.K261695Flowable Restorative Material (KP-Flow LF, KP-Flow MF, KP-Flow HF)Guilin Kevin Peter Technology Co., Ltd.K261485Tetric plus Fill;Tetric plus FlowIvoclar Vivadent, Inc.K262228Transcend Bulk Fill Flowable CompositeUltradent Products, Inc.K261246SRGC-06GC America, 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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