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FDA 510(k)

ESTILUX MICROFILL

K-Number: K780832 · 1978-06-14

ApplicantDegussa Dental, Inc.
Decision Date1978-06-14
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ESTILUX MICROFILL is the device name listed in this FDA 510(k) record. The listed applicant is Degussa Dental, Inc.. It received FDA 510(k) clearance on 1978-06-14 under 510(k) number K780832. 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 ESTILUX MICROFILL?

ESTILUX MICROFILL is a medical device that received FDA 510(k) clearance on 1978-06-14. The listed applicant is Degussa Dental, Inc.. The 510(k) number is K780832.

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

ESTILUX MICROFILL received FDA 510(k) clearance on 1978-06-14, under 510(k) number K780832.

Who is the listed applicant for ESTILUX MICROFILL?

The FDA 510(k) record lists Degussa Dental, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESTILUX MICROFILL?

The FDA product code for ESTILUX MICROFILL is EBF.

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Other records listing Degussa Dental, Inc. as applicant

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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.

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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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