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FDA 510(k)

BELLEGLASS HP OPACEOUS DENTIN

K-Number: K000269 · 2000-03-23

ApplicantSybron Dental Specialties, Inc.
Decision Date2000-03-23
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BELLEGLASS HP OPACEOUS DENTIN is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Dental Specialties, Inc.. It received FDA 510(k) clearance on 2000-03-23 under 510(k) number K000269. 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 BELLEGLASS HP OPACEOUS DENTIN?

BELLEGLASS HP OPACEOUS DENTIN is a medical device that received FDA 510(k) clearance on 2000-03-23. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K000269.

When did BELLEGLASS HP OPACEOUS DENTIN receive FDA 510(k) clearance?

BELLEGLASS HP OPACEOUS DENTIN received FDA 510(k) clearance on 2000-03-23, under 510(k) number K000269.

Who is the listed applicant for BELLEGLASS HP OPACEOUS DENTIN?

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

What is the FDA product code for BELLEGLASS HP OPACEOUS DENTIN?

The FDA product code for BELLEGLASS HP OPACEOUS DENTIN is EBF.

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Other records listing Sybron Dental Specialties, Inc. as applicant

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Related Devices (Code: EBF)

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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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