Cutter Sil-Silicone Impression Mat

FDA 510(k) K760755 · Cutter Laboratories, Inc.

Substantially Equivalent

510(k) numberK760755

Submission

Device name
Cutter Sil-Silicone Impression Mat
Applicant
Cutter Laboratories, Inc.
Mchenry, IL, US
Received
October 1, 1976
Decision date
October 15, 1976
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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K802105C-BladeHWE · Traditional 09/16/1980SE
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Questions and answers

When was Cutter Sil-Silicone Impression Mat cleared by the FDA?

Cutter Sil-Silicone Impression Mat (K760755) received a 510(k) decision of Substantially Equivalent on October 15, 1976, 14 days after the submission was received.

What is the product code of K760755?

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