Sedecal., Sa.
FDA 510(k) medical device clearances.
Top product codes for Sedecal., Sa.
Recent clearances by Sedecal., Sa.
- K232185 — SM-IV
- K222951 — SM-V
- K221803 — PHOENIX/AeroDR TX m01 and PHOENIX/mKDR Xpress.
- K212291 — PHOENIX
- K203537 — Proteus XR/f, Models ST and ET, Multirad and Multirad NET Radiographic Systems
- K202293 — Radiographic System Challenge X
- K192936 — Soltus 500
- K192011 — PhoeniX
- K191813 — MobileDiagnost wDR 2.2
- K173299 — DRAGON X SPSL4HC, DRAGON X SPSL8HC
- K161345 — RadPRO® Mobile 40kW; RadPRO® Mobile 40kW FLEXPLUS, Model SM-40HF-B-D-VIR
- K141895 — MOBILEDIAGNOST WDR
- K133782 — NOVA FA DR SYSTEM
- K130883 — SEDECAL DIGITAL RADIOGRAPHIC UPGRADE MODEL SDRU-T
- K121410 — DRAGON LW
- K101517 — SEDECAL MOBILE DIGITAL DIAGNOSTIC X-RAY
- K111725 — MOBILEDIAGNOST WDR
- K103522 — SEDECAL
- K090322 — EASY MOVING PLUS, SM-XXHF-YY
- K090279 — SEDECAL, MILLENNIUM PLUS
- K090238 — SEDECAL X-PLUS LP PLUS DIGITAL DIAGNOSTIC X-RAY SYSTEMS
- K063283 — DEFINIUM 5000 X-RAY SYSTEM
- K062335 — SEDECAL X PLUS LP PLUS
- K042876 — URS LP DIGITAL, MILLENNIUM, RADPRO
- K043002 — SEDECAL MOBILE X-RAY UNITS WITH DIGITAL DETECTOR
- K020436 — PORTABLE X-RAY UNITS; MODELS SP-HF-2.8 & SP-HF-4.0
Data sourced from openFDA. This site is unofficial and independent of the FDA.