Crystalline L3 Multi-Use Hybrid Composite

FDA 510(k) K935714 · Confi-Dental Products Co.

Substantially Equivalent

510(k) numberK935714

Submission

Device name
Crystalline L3 Multi-Use Hybrid Composite
Applicant
Confi-Dental Products Co.
Louisville, CO, US
Received
November 30, 1993
Decision date
January 21, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DYH – Adhesive, Bracket And Tooth Conditioner, Resin
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3750
Specialty
Dental

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Questions and answers

When was Crystalline L3 Multi-Use Hybrid Composite cleared by the FDA?

Crystalline L3 Multi-Use Hybrid Composite (K935714) received a 510(k) decision of Substantially Equivalent on January 21, 1994, 52 days after the submission was received.

What is the product code of K935714?

The FDA product code is DYH – Adhesive, Bracket And Tooth Conditioner, Resin, a Class II (moderate risk) device regulated under 21 CFR 872.3750.