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FDA 510(k)

IMPROVED TRY-IN GEL

K-Number: K001899 · 2000-08-28

ApplicantSybron Dental Specialties, Inc.
Decision Date2000-08-28
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPROVED TRY-IN GEL 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 2000-08-28 under 510(k) number K001899. 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 IMPROVED TRY-IN GEL?

IMPROVED TRY-IN GEL is a medical device that received FDA 510(k) clearance on 2000-08-28. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K001899.

When did IMPROVED TRY-IN GEL receive FDA 510(k) clearance?

IMPROVED TRY-IN GEL received FDA 510(k) clearance on 2000-08-28, under 510(k) number K001899.

Who is the listed applicant for IMPROVED TRY-IN GEL?

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 IMPROVED TRY-IN GEL?

The FDA product code for IMPROVED TRY-IN GEL is 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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