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FDA 510(k)

4 ALL (DW286A)

K-Number: K020253 · 2002-04-17

ApplicantIvoclar Vivadent, Inc.
Decision Date2002-04-17
Product CodeEJH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

4 ALL (DW286A) is the device name listed in this FDA 510(k) record. The listed applicant is Ivoclar Vivadent, Inc.. It received FDA 510(k) clearance on 2002-04-17 under 510(k) number K020253. The device is classified under product code EJH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 4 ALL (DW286A)?

4 ALL (DW286A) is a medical device that received FDA 510(k) clearance on 2002-04-17. The listed applicant is Ivoclar Vivadent, Inc.. The 510(k) number is K020253.

When did 4 ALL (DW286A) receive FDA 510(k) clearance?

4 ALL (DW286A) received FDA 510(k) clearance on 2002-04-17, under 510(k) number K020253.

Who is the listed applicant for 4 ALL (DW286A)?

The FDA 510(k) record lists Ivoclar Vivadent, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 4 ALL (DW286A)?

The FDA product code for 4 ALL (DW286A) is EJH.

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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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