FDA 510(k) Premarket Notification K061610: PHILIPS MODEL MP20, MP30, MP40, MP50, MP60, MP70, MP80 AND MP90 INTELLIVUE PATIENT MONITORS

Submission Details & Decision

Normalized public record details for 510(k) notification K061610.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K061610

Applicant / Sponsor

Philips Medizin Systeme Boeblingen GmbH

Device Name

PHILIPS MODEL MP20, MP30, MP40, MP50, MP60, MP70, MP80 AND MP90 INTELLIVUE PATIENT MONITORS

Product Code

MHX

Decision Date

2006-08-14

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Cardiovascular (CV)

Clearance Type

Special

Third Party Flag

Date Received

2006-06-09

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