NUK EXPRESSIVETM DOUBLE ELECTRIC BREAST PUMP
K-Number: K121478 · 2013-04-05
Advertisement
Device Summary
Frequently Asked Questions
What is the NUK EXPRESSIVETM DOUBLE ELECTRIC BREAST PUMP?
NUK EXPRESSIVETM DOUBLE ELECTRIC BREAST PUMP is a medical device that received FDA 510(k) clearance on 2013-04-05. The listed applicant is Mapa GmbH. The 510(k) number is K121478.
When did NUK EXPRESSIVETM DOUBLE ELECTRIC BREAST PUMP receive FDA 510(k) clearance?
NUK EXPRESSIVETM DOUBLE ELECTRIC BREAST PUMP received FDA 510(k) clearance on 2013-04-05, under 510(k) number K121478.
Who is the listed applicant for NUK EXPRESSIVETM DOUBLE ELECTRIC BREAST PUMP?
The FDA 510(k) record lists Mapa GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NUK EXPRESSIVETM DOUBLE ELECTRIC BREAST PUMP?
The FDA product code for NUK EXPRESSIVETM 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 Mapa GmbH 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