Atlas FDA

INTELLIVUE GUARDIAN SOFTWARE MODEL 866009, INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216

FDA 510(k) clearance K111905 · decided 2011-10-04

Clearance details

K-number
K111905
Device name
INTELLIVUE GUARDIAN SOFTWARE MODEL 866009, INTELLIVUE CL SP02 POD MODEL 865215, INTELLIVUE CL NBP POD MODEL 865216
Applicant
Philips Medizinsysteme Boeblingen GmbH, Cardiac AN
Decision
Substantially Equivalent
Date received
2011-07-05
Decision date
2011-10-04
Days to decision
91 days
Clearance type
Abbreviated
Product code
DXJ
Device class
2
Regulation number
870.2450
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Boeblingen, Baden-Wuerttemberg, DE
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.