FDA 510(k) Premarket Notification K122439: INTELLIVUE PATIENT MONITOR

Submission Details & Decision

Normalized public record details for 510(k) notification K122439.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K122439

Applicant / Sponsor

Philips Medizin Systeme Boeblingen GmbH

Device Name

INTELLIVUE PATIENT MONITOR

Product Code

MHX

Decision Date

2012-08-29

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Cardiovascular (CV)

Clearance Type

Special

Third Party Flag

Date Received

2012-08-10

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