KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+— 510(k) K030146
Substantially EquivalentKavo America
FDA 510(k) clearance K030146 for KAVO KEY LASER 1242 AND KAVO KEY LASER 1243+, Substantially Equivalent on 2005-08-03. Applicant: Kavo America. Device class: 2.
Clearance details
- Applicant
- Kavo America
- Product code
- Code NVK
- Device class
- Class 2
- Regulation
- 21 CFR 878.4810
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Lake Zurich, IL, US
Recent devices under product code NVK
view all- K253309 — SOGA Lasers therapy system family of Aurora handpiece (Aurora-S) +1 more
- K260765 — Gemini NOVA 810+980 Soft Tissue Laser
- K250731 — MateLaser Medical Diode Laser Systems (ML-DLS-30)
- K243764 — Medical Diode Laser (UTU3-F7B,UTU3-F7W,UTU3-G7B,UTU3-G7W,UTU-G20B,UTU-G20W)
- K230047 — Medical Diode Laser Systems
More clearances from Kavo America
view allData sourced from openFDA. This site is unofficial and independent of the FDA.