FDA 510(k) Premarket Notification K172904: IntelliVue Capnography Extension, IntelliVue Microstream Extension

Submission Details & Decision

Normalized public record details for 510(k) notification K172904.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K172904

Applicant / Sponsor

Philips Medizin Systeme Boeblingen GmbH

Device Name

IntelliVue Capnography Extension, IntelliVue Microstream Extension

Product Code

CCK

Decision Date

2017-12-26

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Anesthesiology (AN)

Clearance Type

Traditional

Third Party Flag

Date Received

2017-09-22

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