Cleared Traditional

K936309 - DELUXE MAGMAG BREAST PUMP

K936309 is an FDA 510(k) clearance for DELUXE MAGMAG BREAST PUMP, manufactured by Pigeon Corp.. The device is a Class 2 Obstetrics & Gynecology device with product code HGX cleared through the Traditional 510(k) pathway after a 394-day FDA review.

K936309 · Pigeon Corp. · Obstetrics & Gynecology device
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Nov 1994
Decision
394d
Days
Class 2
Risk

K936309 is an FDA 510(k) clearance for the DELUXE MAGMAG BREAST PUMP. Classified as Pump, Breast, Powered (product code HGX), Class II - Special Controls.

Submitted by Pigeon Corp. (Tokyo, JP). The FDA issued a Cleared decision on November 30, 1994 after a review of 394 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 Pigeon Corp. devices

FDA 510(k) Submission Details - K936309

510(k) Number K936309 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received November 01, 1993
Decision Date November 30, 1994
Days to Decision 394 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
234d slower than avg
Panel avg: 160d · This submission: 394d
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 210
Devices cleared under the same product code (HGX) and FDA review panel - the closest regulatory comparables to K936309.
WHITE RIVER BATTERY-POWERED BREAST PUMP
K952712 · Natural Technologies, Inc. · Apr 1996
MEDELAS BREAST PUMP
K950750 · Medela, Inc. · Oct 1995
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
MEDELA ELECTRIC BREAST PUMP
K801862 · Medela, Inc. · Oct 1980