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FDA 510(k)

DR BROWN'S NATURAL FLOW DOUBLE ELECTRIC BREAST PUMP, MODEL# 1400

K-Number: K070435 · 2007-07-17

Decision Date2007-07-17
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DR BROWN'S NATURAL FLOW DOUBLE ELECTRIC BREAST PUMP, MODEL# 1400 is the device name listed in this FDA 510(k) record. The listed applicant is Whittlestone, Inc.. It received FDA 510(k) clearance on 2007-07-17 under 510(k) number K070435. 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 DR BROWN'S NATURAL FLOW DOUBLE ELECTRIC BREAST PUMP, MODEL# 1400?

DR BROWN'S NATURAL FLOW DOUBLE ELECTRIC BREAST PUMP, MODEL# 1400 is a medical device that received FDA 510(k) clearance on 2007-07-17. The listed applicant is Whittlestone, Inc.. The 510(k) number is K070435.

When did DR BROWN'S NATURAL FLOW DOUBLE ELECTRIC BREAST PUMP, MODEL# 1400 receive FDA 510(k) clearance?

DR BROWN'S NATURAL FLOW DOUBLE ELECTRIC BREAST PUMP, MODEL# 1400 received FDA 510(k) clearance on 2007-07-17, under 510(k) number K070435.

Who is the listed applicant for DR BROWN'S NATURAL FLOW DOUBLE ELECTRIC BREAST PUMP, MODEL# 1400?

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 DR BROWN'S NATURAL FLOW DOUBLE ELECTRIC BREAST PUMP, MODEL# 1400?

The FDA product code for DR BROWN'S NATURAL FLOW DOUBLE ELECTRIC BREAST PUMP, MODEL# 1400 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.

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.

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.

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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