Mauna Kea Technologies
Mauna Kea Technologies holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2022.
Top product codes for Mauna Kea Technologies
Recent clearances by Mauna Kea Technologies
- K220477 — Cellvizio 100 series system with confocal Miniprobes
- K212322 — Cellvizio I.V.E. system with Confocal Miniprobes
- K193416 — Cellvizio I.V.E. with Confocal Miniprobes
- K191144 — Cellvizio 100 Series System with Confocal Miniprobes
- K183640 — Cellvizio 100 Series Confocal laser Imaging systems and their Confocal Miniprobes
- K180270 — Cellvizio 100 Series Systems with Confocal Miniprobes
- K172844 — Cellvizio 100 Series System with Confocal Miniprobes
- K171345 — Cellvizio 100 Series Systems with Confocal Miniprobes
- K160416 — CystoFlex UHD R-C, CelioFlex UHD 5-C, Cellvizio 100 Series (800) with Confocal Miniprobes
- K150831 — Cellvizio 100 Series System with Confocal Miniprobes
- K151593 — Cellvizio 100 Series System with Confocal Miniprobes
- K141358 — CELLVIZIO 100 SERIES WITH SYSTEM CONFOCAL MINIPROBES
- K133466 — CELLVIZIO 100 SERIES SYSTEM WITH CONFOCAL MINIPROBES (TM)
- K123676 — CELLVIZIO 100 SERIES AND CELLVIZIO SYSTEMS WITH CONFOCAL MINIPROBES
- K122042 — CELLVIZIO 100 SERIES AND CELLVIZIO SYSTEMS WITH CONFOCAL MINIPROBES
- K120208 — CELLVIZIO 100 SERIES SYSTEM AND CELLVIZIO SYSTEM WITH CONFOCAL MINIPROBES
- K061666 — CELLVIZIO WITH CONFOCAL MINIPROBES, MODEL F-600; COLOFLEX AND GASTROFLEX
- K051585 — F-400 SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.