FDA 510(k) Premarket Notification K081793: PHILIPS MP5 AND MP5T INTELLIVUE PATIENT MONITORS AND TRX4841A INTELLIVUE TELEMETRY SYSTEM TRANSCEIVER

Submission Details & Decision

Normalized public record details for 510(k) notification K081793.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K081793

Applicant / Sponsor

Philips Medizin Systeme Boeblingen GmbH

Device Name

PHILIPS MP5 AND MP5T INTELLIVUE PATIENT MONITORS AND TRX4841A INTELLIVUE TELEMETRY SYSTEM TRANSCEIVER

Product Code

MHX

Decision Date

2008-10-14

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Cardiovascular (CV)

Clearance Type

Special

Third Party Flag

Date Received

2008-06-25

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