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FDA 510(k)

WHITTLESTONE BREASTPUMP

K-Number: K002696 · 2001-03-21

ApplicantWhittlestone, Inc.
Decision Date2001-03-21
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

WHITTLESTONE BREASTPUMP is the device name listed in this FDA 510(k) record. The listed applicant is Whittlestone, Inc.. It received FDA 510(k) clearance on 2001-03-21 under 510(k) number K002696. The device is classified under product code HGX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the WHITTLESTONE BREASTPUMP?

WHITTLESTONE BREASTPUMP is a medical device that received FDA 510(k) clearance on 2001-03-21. The listed applicant is Whittlestone, Inc.. The 510(k) number is K002696.

When did WHITTLESTONE BREASTPUMP receive FDA 510(k) clearance?

WHITTLESTONE BREASTPUMP received FDA 510(k) clearance on 2001-03-21, under 510(k) number K002696.

Who is the listed applicant for WHITTLESTONE BREASTPUMP?

The FDA 510(k) record lists Whittlestone, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WHITTLESTONE BREASTPUMP?

The FDA product code for WHITTLESTONE BREASTPUMP is HGX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Whittlestone, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K070435DR BROWN'S NATURAL FLOW DOUBLE ELECTRIC BREAST PUMP, MODEL# 1400K051112WHITTLESTONE EXPRESSER

Related Devices (Code: HGX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K254203Wearable Breast Pump (Model S36)Shenzhen TPH Technology Co., Ltd.K261622Philips Avent Natural Care Hands-free Wearable Electric Breast Pump (Model: SCF593/52, SCF593/62); Philips Avent Natural Care Warming Hands-free Wearable Electric Breast Pump (Model: SCF594/52, SCF594/62)Philips Consumer Lifestyle B.V.K262774Wearable breast pump (Model: XN/MD-2249BS, ZFHF)Guangdong Horigen Mother & Baby Products Co., Ltd.K260643Cimilre Dual MaxCimilre Co., Ltd.K261298Wearable Electric Breast Pump (YM-8837, YM-8838, YM-8856(H03), YM-8809(S42))Guangdong Youmeng Electrical Technology Co., Ltd.K260259DiscreetDuo™ Flow Wearable Breast Pump (Model S3)Shenzhen TPH Technology Co., Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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