Elements

FDA 510(k) K151150 · Pac-Dent International, Inc.

Substantially Equivalent

510(k) numberK151150

Submission

Device name
Elements
Applicant
Pac-Dent International, Inc.
Brea, CA, US
Received
April 30, 2015
Decision date
July 28, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
ELW – Material, Impression
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3660
Specialty
Dental

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Questions and answers

When was Elements cleared by the FDA?

Elements (K151150) received a 510(k) decision of Substantially Equivalent on July 28, 2015, 89 days after the submission was received.

What is the product code of K151150?

The FDA product code is ELW – Material, Impression, a Class II (moderate risk) device regulated under 21 CFR 872.3660.