FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

SMART RAD

K Number: K003438 · Decision Jul 3, 2001
Classifications
1
FEI Numbers
126
Registration Numbers
126
Same Product Code
422
Applicant Total
12
Review Days
239

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Basic Information

Device Name
SMART RAD
K Number
K003438
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cmt Medical Technologies, Ltd.
Date Received
November 6, 2000
Decision Date
July 3, 2001
Product Code
MQB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

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 Cmt Medical Technologies, Ltd.

K Number Device Name
K202235 ArtPIX DRF
K162224 ArtPix Mobile EZ2GO
K110849 PRESTODR 4143
K103038 DUET DRF
K100400 PRESTODR PORTABLE
K080890 SMARTSPOT PRIMAX
K001111 PANORET, MODEL 1000A
K991578 SMARTSPOT 2000
K961140 FLUOROPLUS CARDIAC TV
K961307 SMART SPOT
Search all 12 clearances from Cmt Medical Technologies, Ltd. →