FDA 510(k) Premarket Notification K150310: IntelliVue Patient Monitor

Submission Details & Decision

Normalized public record details for 510(k) notification K150310.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K150310

Applicant / Sponsor

Philips Medizin Systeme Boeblingen GmbH

Device Name

IntelliVue Patient Monitor

Product Code

DSI

Decision Date

2015-05-13

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Cardiovascular (CV)

Clearance Type

Special

Third Party Flag

Date Received

2015-02-09

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