Sapphire Plasma Arc Dental Curing Light

FDA 510(k) K081287 · Den-Mat Holdings, LLC

Substantially Equivalent

510(k) numberK081287

Submission

Device name
Sapphire Plasma Arc Dental Curing Light
Applicant
Den-Mat Holdings, LLC
Santa Maria, CA, US
Received
May 7, 2008
Decision date
November 21, 2008
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 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 Sapphire Plasma Arc Dental Curing Light cleared by the FDA?

Sapphire Plasma Arc Dental Curing Light (K081287) received a 510(k) decision of Substantially Equivalent on November 21, 2008, 198 days after the submission was received.

What is the product code of K081287?

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