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

CT-MASS

K Number: K033774 · Decision Mar 2, 2004
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
17
Review Days
90

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
CT-MASS
K Number
K033774
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medis Medical Imaging Systems BV
Date Received
December 3, 2003
Decision Date
March 2, 2004
Product Code
JAK
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
JAK System, X-Ray, Tomography, Computed

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JAK), ordered by most recent decision date.

View all

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
K042383 RSA-CMS
K041162 ORTHO-CMS
K040746 MRA-CMS
K023970 QUANTITATIVE VASCULAR ANGIOGRAPHY - CMS
Search all 17 clearances from Medis Medical Imaging Systems BV →