KBL Sunlamp Products (= Device Bundling name)— 510(k) K151962
Substantially EquivalentKbl AG
FDA 510(k) clearance K151962 for KBL Sunlamp Products (= Device Bundling name), Substantially Equivalent on 2016-09-15. Applicant: Kbl AG. Device class: 2.
Clearance details
- Applicant
- Kbl AG
- Product code
- Code LEJ
- Device class
- Class 2
- Regulation
- 21 CFR 878.4635
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Dernbach, DE
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Data sourced from openFDA. This site is unofficial and independent of the FDA.