FDA 510(k) Premarket Notification K140771: PHILIPS ELEVA WORKSPOT

Submission Details & Decision

Normalized public record details for 510(k) notification K140771.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K140771

Applicant / Sponsor

Philips Medical Systems Dmc GmbH

Device Name

PHILIPS ELEVA WORKSPOT

Product Code

MQB

Decision Date

2014-04-25

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Radiology (RA)

Clearance Type

Special

Third Party Flag

Date Received

2014-03-27

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