Cleared Traditional

K950750 - MEDELAS BREAST PUMP

K950750 is an FDA 510(k) clearance for MEDELAS BREAST PUMP, manufactured by Medela, Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code HGX cleared through the Traditional 510(k) pathway after a 241-day FDA review.

K950750 · Medela, Inc. · Obstetrics & Gynecology device
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Oct 1995
Decision
241d
Days
Class 2
Risk

K950750 is an FDA 510(k) clearance for the MEDELAS BREAST PUMP. Classified as Pump, Breast, Powered (product code HGX), Class II - Special Controls.

Submitted by Medela, Inc. (Mchenry, US). The FDA issued a Cleared decision on October 16, 1995 after a review of 241 days - an extended review cycle.

This device falls under the Obstetrics & Gynecology FDA review panel, regulated under 21 CFR 884.5160 - the FDA obstetrics and gynecology device framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.

Device pattern: Standard predicate-based submission. Standard predicate reliance. This clearance follows a standard predicate-based equivalence path within the Obstetrics & Gynecology review framework, consistent with the majority of Class II 510(k) submissions.

View all Medela, Inc. devices

FDA 510(k) Submission Details - K950750

510(k) Number K950750 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 17, 1995
Decision Date October 16, 1995
Days to Decision 241 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Statement
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
81d slower than avg
Panel avg: 160d · This submission: 241d
Pathway characteristics
Predicate-based equivalence. No clinical trials required.

HGX Device Classification - Class 2, Special Controls

Product Code HGX Pump, Breast, Powered
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 884.5160
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Obstetrics & Gynecology devices follow this clearance model.

Regulatory Peers - HGX Pump, Breast, Powered

All 162
Devices cleared under the same product code (HGX) and FDA review panel - the closest regulatory comparables to K950750.
WHITE RIVER AUTOMATIC BREAST PUMP
K964679 · White River Concepts · Jun 1997
DOUBLE UP BREAST PUMP
K964396 · The Natural Choice Co., Inc. · Jun 1997
SIMPLICITY TM ELECTRIC/BATTERY BREAST PUMP KIT (1068)
K964403 · The First Years, Inc. · Jan 1997
EGNELL ELITE
K950531 · Hollister, Inc. · Sep 1995
MEDELA BATTERY OPERATED BREAST PUMP
K901344 · Medela, Inc. · Aug 1990
MEDELA BREAST-PUMP LACTINA
K875300 · Medela, Inc. · Apr 1988