FDA 510(k) Premarket Notification K053522: PHILIPS MP40, MP50, MP60, MP70, MP80 AND MP90 INTELLIVUE PATIENT MONITORS, RELEASE D.00

Submission Details & Decision

Normalized public record details for 510(k) notification K053522.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K053522

Applicant / Sponsor

Philips Medizin Systeme Boeblingen GmbH

Device Name

PHILIPS MP40, MP50, MP60, MP70, MP80 AND MP90 INTELLIVUE PATIENT MONITORS, RELEASE D.00

Product Code

MHX

Decision Date

2006-01-10

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Cardiovascular (CV)

Clearance Type

Special

Third Party Flag

Date Received

2005-12-19

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