FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SIREMOBIL ISO-C 3D

K Number: K032280 · Decision Sep 10, 2003
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
235
Applicant Total
15
Review Days
48

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
SIREMOBIL ISO-C 3D
K Number
K032280
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
892.1720
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Siemens AG
Date Received
July 24, 2003
Decision Date
September 10, 2003
Product Code
IZL
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
IZL System, X-Ray, Mobile

Similar 510(k) Clearances

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

View all

Other Clearances by Siemens AG

K Number Device Name
K150843 syngo®.via (version VB10A)
K123375 SYNGO.VIA
K110366 SYNGO.CT CARDIAC FUNCTION
K071310 SYNGO CT ONCOLOGY SOFTWARE PACKAGE
K063507 SYNGO NEURO PBV CT
K063373 FLEX LOOP COIL SET 3T
K053024 SYNGO NEURO DSA CT
K050867 SYNGO BODY PERFUSION-CT
K043122 SMD 21500 OR DSB-2103-D-5MP-5M PIXEL GRAYSCALE FLAT PANEL DISPLAY
K972436 T1 LINE DENTAL HANDPIECES
Search all 15 clearances from Siemens AG →