Plasmacure Bxe

FDA 510(k) K033795 · Eele Laboratories, LLC

Substantially Equivalent

510(k) numberK033795

Submission

Device name
Plasmacure Bxe
Applicant
Eele Laboratories, LLC
Bohemia, NY, US
Received
December 5, 2003
Decision date
December 19, 2003
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

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 Plasmacure Bxe cleared by the FDA?

Plasmacure Bxe (K033795) received a 510(k) decision of Substantially Equivalent on December 19, 2003, 14 days after the submission was received.

What is the product code of K033795?

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