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

Philips Multislice CT System with Low Dose CT Lung Cancer

K Number: K153444 · Decision Apr 8, 2016
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
190
Review Days
133

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
Philips Multislice CT System with Low Dose CT Lung Cancer
K Number
K153444
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Philips Medical Systems (Cleveland), Inc.
Date Received
November 27, 2015
Decision Date
April 8, 2016
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 Philips Medical Systems (Cleveland), Inc.

K Number Device Name
K171850 Philips CT Big Bore
K172406 Ingenuity TF
K162838 Philips iCT CT System
K163711 IQon Spectral CT
K170086 Pinnacle Radiation Therapy Planning System
K160743 Philips Ingenuity CT
K130992 PINNACLE3 RADIATION THERAPY PLANNING SYSTEM
K111336 EBW NM 2.0
K111024 JETPACK 2.0
K092747 PHILIPS COMPREHENSIVE CARDIAC ANALYSIS (CCA) - PLAQUE ASSESSMENT TOOL
Search all 190 clearances from Philips Medical Systems (Cleveland), Inc. →