HANDHELD MANUAL BREAST PUMP (AVENT MANUAL BREAST PUMP)— 510(k) K101538

Name: FDA 510(k) clearance K101538
Creator: U.S. Food and Drug Administration
Published: 2010-11-05

Substantially Equivalent

Philips Electronics UK Limited

FDA 510(k) clearance K101538 for HANDHELD MANUAL BREAST PUMP (AVENT MANUAL BREAST PUMP), Substantially Equivalent on 2010-11-05. Applicant: Philips Electronics UK Limited. Device class: 1.

Clearance details

Applicant: Philips Electronics UK Limited
Product code: Code HGY
Device class: Class 1
Regulation: 21 CFR 884.5150
Advisory panel: Obstetrics/Gynecology
Date received: 2010-06-03
Decision date: 2010-11-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Great Abington, Cambridge, GB

Download summary PDF View on FDA.gov ↗

Recent devices under product code HGY

view all

K032845 — EASY COMFORT DELUXE MANUAL BREAST PUMP, MODEL 11872004-04-05
K013226 — EVENFLO COMFORT EASE MANUAL BREAST PUMP KIT2001-12-20
K011519 — AMEDA HYGIENIKIT2001-08-15
K971231 — WHITE RIVER MINI MANUAL BREAST PUMP1997-05-19
K962828 — EVERT-IT1997-02-10

More clearances from Philips Electronics UK Limited

view all

Data sourced from openFDA. This site is unofficial and independent of the FDA.