SKINTACT— 510(k) K140340
Substantially EquivalentLeonhard Lang GmbH
FDA 510(k) clearance K140340 for SKINTACT, Substantially Equivalent on 2014-05-21. Applicant: Leonhard Lang GmbH. Device class: 2.
Clearance details
- Applicant
- Leonhard Lang GmbH
- Product code
- Code GXY
- Device class
- Class 2
- Regulation
- 21 CFR 882.1320
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stillwater, MN, US
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More clearances from Leonhard Lang GmbH
view allData sourced from openFDA. This site is unofficial and independent of the FDA.