ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100
K-Number: K051413 · 2005-08-29
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Device Summary
Frequently Asked Questions
What is the ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100?
ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100 is a medical device that received FDA 510(k) clearance on 2005-08-29. The listed applicant is Avent America, Inc.. The 510(k) number is K051413.
When did ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100 receive FDA 510(k) clearance?
ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100 received FDA 510(k) clearance on 2005-08-29, under 510(k) number K051413.
Who is the listed applicant for ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100?
The FDA 510(k) record lists Avent America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100?
The FDA product code for ISIS IQ DUO TWIN ELECTRONIC BREAST PUMP, MODEL 100 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 Avent America, 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.
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