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

MODIFICATION TO SECTRA IDS5 RADIOLOGY WORKSTATION - VERSION 10.1

K Number: K033712 · Decision Dec 23, 2003
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
9
Review Days
27

Basic Information

Device Name
MODIFICATION TO SECTRA IDS5 RADIOLOGY WORKSTATION - VERSION 10.1
K Number
K033712
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
November 26, 2003
Decision Date
December 23, 2003
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.

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Other Clearances by SECTRA-IMTEC AB

K Number Device Name
K040376 SECTRA IDS5 RADIOLOGY WORKSTATION; SECTRA MPR PACKAGE; SECTRA 3D PACKAGE
K031590 SECTRA ORTHOPEDIC PACKAGE
K021527 SECTRA OSTEOPOROSIS PACKAGE
K002936 MODIFICATION TO IDS5 IMAGE DISPLAY SYSTEM
K983447 WISE (II) IMAGE MANAGEMENT SYSTEM
K965161 SMIIC (SECTRA MEDICAL IMAGE INPUT CONTROLLER)
K963395 IMAGESERVER 2000 PICTURE ARCHIVING SYSTEM
K961983 TRS 2000 TELERADIOLOGY SYSTEM