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FDA 510(k)

LC MICROFILL

K-Number: K991442 · 1999-06-03

ApplicantS & C Polymer GmbH
Decision Date1999-06-03
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LC MICROFILL is the device name listed in this FDA 510(k) record. The listed applicant is S & C Polymer GmbH. It received FDA 510(k) clearance on 1999-06-03 under 510(k) number K991442. 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 LC MICROFILL?

LC MICROFILL is a medical device that received FDA 510(k) clearance on 1999-06-03. The listed applicant is S & C Polymer GmbH. The 510(k) number is K991442.

When did LC MICROFILL receive FDA 510(k) clearance?

LC MICROFILL received FDA 510(k) clearance on 1999-06-03, under 510(k) number K991442.

Who is the listed applicant for LC MICROFILL?

The FDA 510(k) record lists S & C Polymer GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LC MICROFILL?

The FDA product code for LC MICROFILL is EBF.

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Other records listing S & C Polymer GmbH 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: 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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