Sternvantage Varnish LC, Model 221001

FDA 510(k) K984341 · Sterngold/Implamed

Substantially Equivalent

510(k) numberK984341

Submission

Device name
Sternvantage Varnish LC, Model 221001
Applicant
Sterngold/Implamed
Attleboro, MA, US
Received
December 4, 1998
Decision date
January 8, 1999
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EBI – Resin, Denture, Relining, Repairing, Rebasing
Device class
Class II (moderate risk)
Regulation
21 CFR 872.3760
Specialty
Dental

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Questions and answers

When was Sternvantage Varnish LC, Model 221001 cleared by the FDA?

Sternvantage Varnish LC, Model 221001 (K984341) received a 510(k) decision of Substantially Equivalent on January 8, 1999, 35 days after the submission was received.

What is the product code of K984341?

The FDA product code is EBI – Resin, Denture, Relining, Repairing, Rebasing, a Class II (moderate risk) device regulated under 21 CFR 872.3760.