Kub Technologies, Inc.
Kub Technologies, Inc. holds FDA 510(k) medical device clearances, first cleared 2007, most recent 2021.
Top product codes for Kub Technologies, Inc.
Recent clearances by Kub Technologies, Inc.
- K210955 — Kubtec Mozart Supra (XPERT 84) Radiography System
- K210956 — Kubtec Mozart (XPERT42)
- K210957 — Kubec Xpert 80 Radiography System
- K200756 — Kubtec Mozart Supra
- K183624 — Kubtec Mozart (Xpert42)
- K151221 — Kubtec DIGIVIEW 395
- K141539 — KUBTEC X250
- K103348 — DIGIVIEW 250
- K083510 — KUBTEC XPERT 20
- K071233 — XPERT 40 SPECIMEN RADIOGRAPHY SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.