System Plus

FDA 510(k) K073475 · Continental Dental Laboratory

Substantially Equivalent

510(k) numberK073475

Submission

Device name
System Plus
Applicant
Continental Dental Laboratory
Torrance, CA, US
Received
December 11, 2007
Decision date
March 10, 2008
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

Other 510(k)s with product code ELW

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K233954Chemi-SiL (HB, MB, LB, LBS); Chemi-SiL Bite-BluELW · Traditional B&E Korea Co., Ltd.02/13/2024SE
K223892DentMix VPS Impression MaterialELW · Traditional Innovative Product Brands, Inc.04/27/2023SE
K213175No Stress ImpressELW · Traditional No Stress Impress, LLC01/19/2023SE
K214086Bright Impress-Light, Bright Impress-Medium, Bright Impress-Heavy, Bright Impress-Bite…ELW · Traditional Genoss Co., Ltd.12/15/2022SE
K222741DENU Light Body(Regular, Fast), DENU Heavy Body(Regular, Fast), DENU Putty Set(Regular…ELW · Traditional Hdi, Inc.11/07/2022SE

Questions and answers

When was System Plus cleared by the FDA?

System Plus (K073475) received a 510(k) decision of Substantially Equivalent on March 10, 2008, 90 days after the submission was received.

What is the product code of K073475?

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