NELLCOR PORTABLE SPO2 PATIENT MONITORING SYSTEM ( NPSPMS )

FDA 510(k) Premarket Notification · Submission K141542 · Applicant: Covidien, LLC

Public Record 510(k) Submission Decision Date: 2014-10-02 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K141542.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K141542
Applicant / Sponsor
Device Name
NELLCOR PORTABLE SPO2 PATIENT MONITORING SYSTEM ( NPSPMS )
Product Code
DQA
Decision Date
2014-10-02
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Cardiovascular (CV)
Clearance Type
Traditional
Third Party Flag
N
Date Received
2014-06-10

Related Establishments / Registrations

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