Konica Minolta, Inc.
FDA 510(k) medical device clearances.
Top product codes for Konica Minolta, Inc.
Recent clearances by Konica Minolta, Inc.
- K250665 — SKR 3000
- K241319 — SKR 3000
- K240281 — Bone Suppression Software
- K230906 — Konicaminolta DI-X1
- K223267 — SKR 3000
- K220993 — Ultrasound System SONIMAGE MX1
- K213908 — SKR 3000
- K212685 — KONICAMINOLTA DI-X1
- K210619 — SKR 3000
- K210066 — ImagePilot
- K191645 — SKR 4000
- K182688 — SKR 3000
- K182431 — Konicaminolta DI-X1
- K182153 — Ultrasound System SONIMAGE HS1
- K180084 — Ultrasound System SONIMAGE MX1
- K172793 — SKR 3000
- K171716 — SKR 3000
- K162065 — Ultrasound System SONIMAGE HS1
- K162504 — SKR 3000
- K152577 — ULTRASOUND SYSTEM SONIMAGE HS 1
- K151465 — AeroDR SYSTEM 2
- K151060 — Ultrasound System SONIMAGE HS1
- K142197 — ULTRASOUND SYSTEM SONIMAGE HS1, LINEAR PROBE L18-4, CONVEX PROBE C5-2
- K141271 — AERODR SYSTEM 2
- K133730 — CO PILOT/REGIUS UNITEA
Data sourced from openFDA. This site is unofficial and independent of the FDA.