Mauna Kea Technologies
FDA 510(k) medical device clearances.
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.