FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

XP202

K Number: K161922 · Decision Sep 1, 2016
Classifications
1
FEI Numbers
158
Registration Numbers
158
Same Product Code
481
Applicant Total
12
Review Days
50

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Basic Information

Device Name
XP202
K Number
K161922
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.6660
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
3M Deutschland GmbH
Date Received
July 13, 2016
Decision Date
September 1, 2016
Product Code
EIH
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
EIH Powder, Porcelain

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K151748 Clean & More
K151144 SuPro 100
K140684 CLINPRO PROPHY POWDER
K133436 FLASH AR; FLASH AR QUICK
K131404 FLASH AR PENTA / FLASH AR PENTA QUICK
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