XP202— 510(k) K161922
Substantially Equivalent3M Deutschland GmbH
FDA 510(k) clearance K161922 for XP202, Substantially Equivalent on 2016-09-01. Applicant: 3M Deutschland GmbH. Device class: 2.
Clearance details
- Applicant
- 3M Deutschland GmbH
- Product code
- Code EIH
- Device class
- Class 2
- Regulation
- 21 CFR 872.6660
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Seefeld, DE
Recent devices under product code EIH
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