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

MODIFICATION TO IDS5 IMAGE DISPLAY SYSTEM

K Number: K002936 · Decision Oct 17, 2000
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
9
Review Days
26

Basic Information

Device Name
MODIFICATION TO IDS5 IMAGE DISPLAY SYSTEM
K Number
K002936
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
SECTRA-IMTEC AB
Date Received
September 21, 2000
Decision Date
October 17, 2000
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

Similar 510(k) Clearances

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

View all

Other Clearances by SECTRA-IMTEC AB

K Number Device Name
K040376 SECTRA IDS5 RADIOLOGY WORKSTATION; SECTRA MPR PACKAGE; SECTRA 3D PACKAGE
K033712 MODIFICATION TO SECTRA IDS5 RADIOLOGY WORKSTATION - VERSION 10.1
K031590 SECTRA ORTHOPEDIC PACKAGE
K021527 SECTRA OSTEOPOROSIS PACKAGE
K983447 WISE (II) IMAGE MANAGEMENT SYSTEM
K965161 SMIIC (SECTRA MEDICAL IMAGE INPUT CONTROLLER)
K963395 IMAGESERVER 2000 PICTURE ARCHIVING SYSTEM
K961983 TRS 2000 TELERADIOLOGY SYSTEM