LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002
K-Number: K021739 · 2003-01-10
Advertisement
Device Summary
Frequently Asked Questions
What is the LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002?
LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002 is a medical device that received FDA 510(k) clearance on 2003-01-10. The listed applicant is Limerick, Inc.. The 510(k) number is K021739.
When did LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002 receive FDA 510(k) clearance?
LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002 received FDA 510(k) clearance on 2003-01-10, under 510(k) number K021739.
Who is the listed applicant for LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002?
The FDA 510(k) record lists Limerick, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002?
The FDA product code for LIMERICK POWERED ELECTRIC BREAST PUMP MODEL 1002 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 Limerick, 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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
Advertisement