Mothers Touch One Hand Breast Pump

FDA 510(k) K912355 · Hollister, Inc.

Substantially Equivalent

510(k) numberK912355

Submission

Device name
Mothers Touch One Hand Breast Pump
Applicant
Hollister, Inc.
Chicago, IL, US
Received
May 28, 1991
Decision date
December 10, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
HGY – Pump, Breast, Non-Powered
Device class
Class I (low risk)
Regulation
21 CFR 884.5150
Specialty
Obstetrics/Gynecology

Other 510(k)s with product code HGY

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K101538Handheld Manual Breast Pump (Avent Manual Breast Pump)HGY · Traditional Philips Electronics UK Limited11/05/2010SE
K032845Easy Comfort Deluxe Manual Breast Pump, Model 1187HGY · Traditional The First Years, Inc.04/05/2004SE
K013226Evenflo Comfort Ease Manual Breast Pump KitHGY · Traditional Evenflo Company, Inc.12/20/2001SE
K011519Ameda HygienikitHGY · Traditional Hollister, Inc.08/15/2001SE
K971231White River Mini Manual Breast PumpHGY · Traditional White River Concepts05/19/1997SE
K962828Evert-ItHGY · Traditional Genesis Industries, Inc.02/10/1997SE
K952034Medela's Foot PumpHGY · Traditional Medela, Inc.09/12/1995SE
K952035NipletteHGY · Traditional Avent America, Inc.07/28/1995SE
K925738White River Manual Breast PumpHGY · Traditional White River (Tm)05/04/1994SE
K902552Gerber Precious Care Electric Breast PumpHGY · Traditional Gerber Products Co.09/26/1990SE

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Questions and answers

When was Mothers Touch One Hand Breast Pump cleared by the FDA?

Mothers Touch One Hand Breast Pump (K912355) received a 510(k) decision of Substantially Equivalent on December 10, 1993, 927 days after the submission was received.

What is the product code of K912355?

The FDA product code is HGY – Pump, Breast, Non-Powered, a Class I (low risk) device regulated under 21 CFR 884.5150.