CARE ELECTRIC BREAST PUMP
K-Number: K844013 · 1985-02-15
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Device Summary
Frequently Asked Questions
What is the CARE ELECTRIC BREAST PUMP?
CARE ELECTRIC BREAST PUMP is a medical device that received FDA 510(k) clearance on 1985-02-15. The listed applicant is Hankscraft Div. of Gerber Products Co.. The 510(k) number is K844013.
When did CARE ELECTRIC BREAST PUMP receive FDA 510(k) clearance?
CARE ELECTRIC BREAST PUMP received FDA 510(k) clearance on 1985-02-15, under 510(k) number K844013.
Who is the listed applicant for CARE ELECTRIC BREAST PUMP?
The FDA 510(k) record lists Hankscraft Div. of Gerber Products Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CARE ELECTRIC BREAST PUMP?
The FDA product code for CARE 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 Hankscraft Div. of 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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