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FDA 510(k)

LIFE 2

K-Number: K012717 · 2001-10-25

ApplicantSybron Dental Specialties, Inc.
Decision Date2001-10-25
Product CodeEJK
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LIFE 2 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 2001-10-25 under 510(k) number K012717. The device is classified under product code EJK. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIFE 2?

LIFE 2 is a medical device that received FDA 510(k) clearance on 2001-10-25. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K012717.

When did LIFE 2 receive FDA 510(k) clearance?

LIFE 2 received FDA 510(k) clearance on 2001-10-25, under 510(k) number K012717.

Who is the listed applicant for LIFE 2?

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 LIFE 2?

The FDA product code for LIFE 2 is EJK.

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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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