INTELLIVUE PATIENT MONITORS WITH RELEASE C.02, MODELS MP20, MP30, MP40, MP50, MP60, MP70, MP80 AND MP90

FDA 510(k) Premarket Notification · Submission K052801 · Applicant: Philips Medizin Systeme Boeblingen GmbH

Public Record 510(k) Submission Decision Date: 2005-11-02 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K052801.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K052801
Device Name
INTELLIVUE PATIENT MONITORS WITH RELEASE C.02, MODELS MP20, MP30, MP40, MP50, MP60, MP70, MP80 AND MP90
Product Code
MHX
Decision Date
2005-11-02
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Cardiovascular (CV)
Clearance Type
Special
Third Party Flag
N
Date Received
2005-10-03

Related Establishments / Registrations

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