Cleared Traditional

K960727 - EVENFLO NATURAL MOTHER ELECTRIC BREAST PUMP KIT

K960727 is an FDA 510(k) clearance for EVENFLO NATURAL MOTHER ELECTRIC BREAST ..., manufactured by Evenflo Co., Inc.. The device is a Class 2 Obstetrics & Gynecology device with product code HGX cleared through the Traditional 510(k) pathway after a 358-day FDA review.

K960727 · Evenflo Co., Inc. · Obstetrics & Gynecology device
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Feb 1997
Decision
358d
Days
Class 2
Risk

K960727 is an FDA 510(k) clearance for the EVENFLO NATURAL MOTHER ELECTRIC BREAST PUMP KIT. Classified as Pump, Breast, Powered (product code HGX), Class II - Special Controls.

Submitted by Evenflo Co., Inc. (Washington D.C., US). The FDA issued a Cleared decision on February 14, 1997 after a review of 358 days - an unusually long review period, suggesting complex equivalence evaluation.

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. Elevated predicate reliance profile. 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 Evenflo Co., Inc. devices

FDA 510(k) Submission Details - K960727

510(k) Number K960727 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received February 22, 1996
Decision Date February 14, 1997
Days to Decision 358 days
Submission Type Traditional
Review Panel Obstetrics & Gynecology (OB)
Summary Statement
Third-party Review No - reviewed directly by FDA
Regulatory Context
Review time vs. panel average
198d slower than avg
Panel avg: 160d · This submission: 358d
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 166
Devices cleared under the same product code (HGX) and FDA review panel - the closest regulatory comparables to K960727.
LUXMATIC 12-15 ISC PORTABLE ELECTRIC BREAST PUMP
K971543 · Kaweco GmbH · Sep 1997
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
WHITE RIVER BATTERY-POWERED BREAST PUMP
K952712 · Natural Technologies, Inc. · Apr 1996
MEDELAS BREAST PUMP
K950750 · Medela, Inc. · Oct 1995