FDA 510(k) FDA class 2 Substantially Equivalent 🇳🇱 Netherlands

RSA-CMS

K Number: K042383 · Decision Oct 20, 2004
Classifications
1
FEI Numbers
599
Registration Numbers
599
Same Product Code
2271
Applicant Total
17
Review Days
49

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Basic Information

Device Name
RSA-CMS
K Number
K042383
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medis Medical Imaging Systems BV
Date Received
September 1, 2004
Decision Date
October 20, 2004
Product Code
LLZ
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
LLZ System, Image Processing, Radiological

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Other Clearances by Medis Medical Imaging Systems BV

K Number Device Name
K182611 Qangio XA 3D
K140587 MR-CT VVA
K112807 X-RAY VVA
K073156 QPLAQUE MR
K062386 QANGIO CT
K050703 QBRAIN
K041162 ORTHO-CMS
K040746 MRA-CMS
K033774 CT-MASS
K023970 QUANTITATIVE VASCULAR ANGIOGRAPHY - CMS
Search all 17 clearances from Medis Medical Imaging Systems BV →