Ultrafine Tray Adhesive

FDA 510(k) K820489 · Buffalo Dental Mfg. Co., Inc.

Substantially Equivalent

510(k) numberK820489

Submission

Device name
Ultrafine Tray Adhesive
Applicant
Buffalo Dental Mfg. Co., Inc.
Mchenry, IL, US
Received
February 23, 1982
Decision date
March 19, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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

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K841491Conventional Plastic Dental TraysEHY · Traditional 07/13/1984SE
K841490Polysulfide Custom Tray MaterialELW · Traditional 06/27/1984SE
K841323Fuzzy TrayEHY · Traditional 06/27/1984SE
K820216Ultra-WetELW · Traditional 02/24/1982SE
K802990Alginate/Silicone Crown & Bridge MaterELW · Traditional 02/02/1981SE
K802882Hydrocolloid Compatible Cream AlginateELW · Traditional 01/28/1981SE
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Questions and answers

When was Ultrafine Tray Adhesive cleared by the FDA?

Ultrafine Tray Adhesive (K820489) received a 510(k) decision of Substantially Equivalent on March 19, 1982, 24 days after the submission was received.

What is the product code of K820489?

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