3M M.G. Material

FDA 510(k) K981325 · 3M Company

Substantially Equivalent

510(k) numberK981325

Submission

Device name
3M M.G. Material
Applicant
3M Company
St. Paul, MN, US
Received
April 13, 1998
Decision date
June 11, 1998
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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 3M M.G. Material cleared by the FDA?

3M M.G. Material (K981325) received a 510(k) decision of Substantially Equivalent on June 11, 1998, 59 days after the submission was received.

What is the product code of K981325?

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