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FDA 510(k)

LEE-FILL ULTRAVIOLET-CURED REST. MAT.

K-Number: K760417 · 1976-08-23

ApplicantLee Pharmaceuticals
Decision Date1976-08-23
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LEE-FILL ULTRAVIOLET-CURED REST. MAT. is the device name listed in this FDA 510(k) record. The listed applicant is Lee Pharmaceuticals. It received FDA 510(k) clearance on 1976-08-23 under 510(k) number K760417. 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 LEE-FILL ULTRAVIOLET-CURED REST. MAT.?

LEE-FILL ULTRAVIOLET-CURED REST. MAT. is a medical device that received FDA 510(k) clearance on 1976-08-23. The listed applicant is Lee Pharmaceuticals. The 510(k) number is K760417.

When did LEE-FILL ULTRAVIOLET-CURED REST. MAT. receive FDA 510(k) clearance?

LEE-FILL ULTRAVIOLET-CURED REST. MAT. received FDA 510(k) clearance on 1976-08-23, under 510(k) number K760417.

Who is the listed applicant for LEE-FILL ULTRAVIOLET-CURED REST. MAT.?

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

What is the FDA product code for LEE-FILL ULTRAVIOLET-CURED REST. MAT.?

The FDA product code for LEE-FILL ULTRAVIOLET-CURED REST. MAT. is EBF.

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Other records listing Lee Pharmaceuticals 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.

K924378RESTOBOND 4K912256PRECISE(R) BETA QUARTZ GLASS-CERAMIC INSERTK900809LEE-FISCHER CERAMIC REINFORCED PLASTIC BRACKETSK894315RESTOBOND 3/DENTIN-ENAMEL BONDING AGENTK881903PROSTHODENT VLK873123LEE COMPOSITE INLAY SYSTEM

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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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