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FDA 510(k)

OPTIBAND LC

K-Number: K032407 · 2003-10-06

ApplicantSybron Dental Specialties, Inc.
Decision Date2003-10-06
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

OPTIBAND LC 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 2003-10-06 under 510(k) number K032407. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTIBAND LC?

OPTIBAND LC is a medical device that received FDA 510(k) clearance on 2003-10-06. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K032407.

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

OPTIBAND LC received FDA 510(k) clearance on 2003-10-06, under 510(k) number K032407.

Who is the listed applicant for OPTIBAND LC?

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 OPTIBAND LC?

The FDA product code for OPTIBAND LC is DYH.

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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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