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

BRAIN PERFUSION OPTION

K Number: K033677 · Decision Feb 20, 2004
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
190
Review Days
88

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Basic Information

Device Name
BRAIN PERFUSION OPTION
K Number
K033677
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 24, 2003
Decision Date
February 20, 2004
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

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