Coltene Coltex/Coltoflax

FDA 510(k) K811666 · Coltene, Inc.

Substantially Equivalent

510(k) numberK811666

Submission

Device name
Coltene Coltex/Coltoflax
Applicant
Coltene, Inc.
Mchenry, IL, US
Received
June 15, 1981
Decision date
July 15, 1981
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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Questions and answers

When was Coltene Coltex/Coltoflax cleared by the FDA?

Coltene Coltex/Coltoflax (K811666) received a 510(k) decision of Substantially Equivalent on July 15, 1981, 30 days after the submission was received.

What is the product code of K811666?

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