Palatray LC Resin Impression Tray Material

FDA 510(k) K902350 · Kulzer, Inc.

Substantially Equivalent

510(k) numberK902350

Submission

Device name
Palatray LC Resin Impression Tray Material
Applicant
Kulzer, Inc.
Irvine, CA, US
Received
May 25, 1990
Decision date
July 26, 1990
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
EBH – Material, Impression Tray, Resin
Device class
Class I (low risk)
Regulation
21 CFR 872.3670
Specialty
Dental

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K923979LC Tray MaterialEBH · Traditional Dentsply Intl.11/17/1992SE
K923549Paladisc LCEBH · Traditional Heraeus Kulzer, Inc.09/29/1992SE
K912820Polyester Resin Hand Molded TrayEBH · Traditional E&D Dental Products, Inc.08/21/1991SE
K905058Palavit LEBH · Traditional Kulzer, Inc.06/06/1991SE
K901782Convertray Custom Impression Tray Material SystemEBH · Traditional Productivity Training Corp.06/29/1990SE
K890712Advantage Dental Cust Dent Impress/Baseplate TraysEBH · Traditional Advantage Dental Products, Inc.04/25/1989SE
K881838Modified Permagum AdhesiveEBH · Traditional Espe GmbH (Us)07/27/1988SE
K875257Impregum F AdhesiveEBH · Traditional Espe GmbH (Us)03/09/1988SE

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Questions and answers

When was Palatray LC Resin Impression Tray Material cleared by the FDA?

Palatray LC Resin Impression Tray Material (K902350) received a 510(k) decision of Substantially Equivalent on July 26, 1990, 62 days after the submission was received.

What is the product code of K902350?

The FDA product code is EBH – Material, Impression Tray, Resin, a Class I (low risk) device regulated under 21 CFR 872.3670.