Power LED

FDA 510(k) K033697 · Dental Products of USA, Inc.

Substantially Equivalent

510(k) numberK033697

Submission

Device name
Power LED
Applicant
Dental Products of USA, Inc.
Miami, FL, US
Received
November 25, 2003
Decision date
February 27, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EBZ – Activator, Ultraviolet, For Polymerization
Device class
Class II (moderate risk)
Regulation
21 CFR 872.6070
Specialty
Dental

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Questions and answers

When was Power LED cleared by the FDA?

Power LED (K033697) received a 510(k) decision of Substantially Equivalent on February 27, 2004, 94 days after the submission was received.

What is the product code of K033697?

The FDA product code is EBZ – Activator, Ultraviolet, For Polymerization, a Class II (moderate risk) device regulated under 21 CFR 872.6070.