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FDA 510(k)

GERBER DOUBLE ELECTRIC BREAST PUMP

K-Number: K043098 · 2004-12-15

Decision Date2004-12-15
Product CodeHGX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GERBER DOUBLE ELECTRIC BREAST PUMP is the device name listed in this FDA 510(k) record. The listed applicant is Gerber Products Co.. It received FDA 510(k) clearance on 2004-12-15 under 510(k) number K043098. 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 GERBER DOUBLE ELECTRIC BREAST PUMP?

GERBER DOUBLE ELECTRIC BREAST PUMP is a medical device that received FDA 510(k) clearance on 2004-12-15. The listed applicant is Gerber Products Co.. The 510(k) number is K043098.

When did GERBER DOUBLE ELECTRIC BREAST PUMP receive FDA 510(k) clearance?

GERBER DOUBLE ELECTRIC BREAST PUMP received FDA 510(k) clearance on 2004-12-15, under 510(k) number K043098.

Who is the listed applicant for GERBER DOUBLE ELECTRIC BREAST PUMP?

The FDA 510(k) record lists Gerber Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GERBER DOUBLE ELECTRIC BREAST PUMP?

The FDA product code for GERBER DOUBLE ELECTRIC BREAST PUMP 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 Gerber Products Co. 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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