Philips Electronics UK Limited is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Philips Electronics UK Limited - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Philips Electronics UK Limited has 3 FDA 510(k) cleared medical devices. Based in Houston, US.
Historical record: 3 cleared submissions from 2009 to 2010.
Browse the FDA 510(k) cleared devices submitted by Philips Electronics UK Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Philips Electronics UK Limited
3 devices
Cleared
Nov 05, 2010
HANDHELD MANUAL BREAST PUMP (AVENT MANUAL BREAST PUMP)
Obstetrics & Gynecology
155d
Cleared
Jun 22, 2010
PHILIPS AVENT DIGITAL THERMOMETER SET, MODEL SCH540
General Hospital
123d
Cleared
Jun 18, 2009
PHILIPS AVENT CLASSIC STAGE 2 AND 3 TEETHER, MODEL SCF882/01, SCF884/01,...
Dental
147d