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

PHILIPS INTEGRIS 3D RA OPTION

K Number: K983877 · Decision Dec 21, 1998
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
195
Applicant Total
71
Review Days
49

Basic Information

Device Name
PHILIPS INTEGRIS 3D RA OPTION
K Number
K983877
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1600
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PHILIPS MEDICAL SYSTEMS NORTH AMERICA, INC.
Date Received
November 2, 1998
Decision Date
December 21, 1998
Product Code
IZI
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
IZI System, X-Ray, Angiographic

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