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

HEARTNAVIGATOR RELEASE 1

K Number: K111245 · Decision Jul 29, 2011
Classifications
1
FEI Numbers
609
Registration Numbers
609
Same Product Code
2221
Applicant Total
25
Review Days
87

Basic Information

Device Name
HEARTNAVIGATOR RELEASE 1
K Number
K111245
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
892.2050
Medical Specialty
Radiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Date Received
May 3, 2011
Decision Date
July 29, 2011
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

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