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

WIRELESS PORTABLE DETECTOR FD-W17

K Number: K090625 · Decision Mar 24, 2009
Classifications
1
FEI Numbers
128
Registration Numbers
128
Same Product Code
418
Applicant Total
24
Review Days
15

Basic Information

Device Name
WIRELESS PORTABLE DETECTOR FD-W17
K Number
K090625
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1680
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA CO.
Date Received
March 9, 2009
Decision Date
March 24, 2009
Product Code
MQB
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MQB Solid State X-Ray Imager (Flat Panel/Digital Imager)

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