PHILIPS SP02 DISPOSABLE SENSOR, MODEL M1131A

FDA 510(k) Premarket Notification · Submission K042306 · Applicant: Philips Medizin Systeme Boeblingen GmbH

Public Record 510(k) Submission Decision Date: 2004-10-15 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K042306.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K042306
Device Name
PHILIPS SP02 DISPOSABLE SENSOR, MODEL M1131A
Product Code
DQA
Decision Date
2004-10-15
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Cardiovascular (CV)
Clearance Type
Abbreviated
Third Party Flag
N
Date Received
2004-08-25

Related Establishments / Registrations

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