LANSINOH POWERED ELECTRIC BREAST PUMP
K-Number: K122474 · 2012-12-28
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Device Summary
Frequently Asked Questions
What is the LANSINOH POWERED ELECTRIC BREAST PUMP?
LANSINOH POWERED ELECTRIC BREAST PUMP is a medical device that received FDA 510(k) clearance on 2012-12-28. The listed applicant is Lansinoh Laboratories Saglik Gerecleri Tasarim San. The 510(k) number is K122474.
When did LANSINOH POWERED ELECTRIC BREAST PUMP receive FDA 510(k) clearance?
LANSINOH POWERED ELECTRIC BREAST PUMP received FDA 510(k) clearance on 2012-12-28, under 510(k) number K122474.
Who is the listed applicant for LANSINOH POWERED ELECTRIC BREAST PUMP?
The FDA 510(k) record lists Lansinoh Laboratories Saglik Gerecleri Tasarim San as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LANSINOH POWERED ELECTRIC BREAST PUMP?
The FDA product code for LANSINOH POWERED 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.
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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