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FDA 510(k)

NEXUS 2 CLEAR

K-Number: K013609 · 2002-01-16

ApplicantSybron Dental Specialties, Inc.
Decision Date2002-01-16
Product CodeEMA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

NEXUS 2 CLEAR 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 2002-01-16 under 510(k) number K013609. The device is classified under product code EMA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEXUS 2 CLEAR?

NEXUS 2 CLEAR is a medical device that received FDA 510(k) clearance on 2002-01-16. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K013609.

When did NEXUS 2 CLEAR receive FDA 510(k) clearance?

NEXUS 2 CLEAR received FDA 510(k) clearance on 2002-01-16, under 510(k) number K013609.

Who is the listed applicant for NEXUS 2 CLEAR?

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 NEXUS 2 CLEAR?

The FDA product code for NEXUS 2 CLEAR is EMA.

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Related Devices (Code: EMA)

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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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