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FDA 510(k)

DAMON FT

K-Number: K032408 · 2003-10-15

ApplicantSybron Dental Specialties, Inc.
Decision Date2003-10-15
Product CodeDYW
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DAMON FT 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 2003-10-15 under 510(k) number K032408. The device is classified under product code DYW. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAMON FT?

DAMON FT is a medical device that received FDA 510(k) clearance on 2003-10-15. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K032408.

When did DAMON FT receive FDA 510(k) clearance?

DAMON FT received FDA 510(k) clearance on 2003-10-15, under 510(k) number K032408.

Who is the listed applicant for DAMON FT?

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 DAMON FT?

The FDA product code for DAMON FT is DYW.

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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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