FDA 510(k) FDA class 2 Substantially Equivalent 🇪🇸 Spain

SEDECAL DIGITAL RADIOGRAPHIC UPGRADE MODEL SDRU-T

K Number: K130883 · Decision Apr 18, 2013
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
26
Review Days
20

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Basic Information

Device Name
SEDECAL DIGITAL RADIOGRAPHIC UPGRADE MODEL SDRU-T
K Number
K130883
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sedecal., Sa.
Date Received
March 29, 2013
Decision Date
April 18, 2013
Product Code
MQB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

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Other Clearances by Sedecal., Sa.

K Number Device Name
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
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