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FDA 510(k)

LEE COMPOSITE INLAY SYSTEM

K-Number: K873123 · 1988-01-20

ApplicantLee Pharmaceuticals
Decision Date1988-01-20
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LEE COMPOSITE INLAY SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Lee Pharmaceuticals. It received FDA 510(k) clearance on 1988-01-20 under 510(k) number K873123. 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 COMPOSITE INLAY SYSTEM?

LEE COMPOSITE INLAY SYSTEM is a medical device that received FDA 510(k) clearance on 1988-01-20. The listed applicant is Lee Pharmaceuticals. The 510(k) number is K873123.

When did LEE COMPOSITE INLAY SYSTEM receive FDA 510(k) clearance?

LEE COMPOSITE INLAY SYSTEM received FDA 510(k) clearance on 1988-01-20, under 510(k) number K873123.

Who is the listed applicant for LEE COMPOSITE INLAY SYSTEM?

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 COMPOSITE INLAY SYSTEM?

The FDA product code for LEE COMPOSITE INLAY SYSTEM 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 VLK863157RESTODENT POSTERIOR

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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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