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FDA 510(k)

Emily's Care Nourish Test System (Model 1)

K-Number: K234088 · 2024-05-03

Decision Date2024-05-03
Product CodeQEI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Emily's Care Nourish Test System (Model 1) is the device name listed in this FDA 510(k) record. The listed applicant is Lactation Lab, Inc.. It received FDA 510(k) clearance on 2024-05-03 under 510(k) number K234088. The device is classified under product code QEI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Emily's Care Nourish Test System (Model 1)?

Emily's Care Nourish Test System (Model 1) is a medical device that received FDA 510(k) clearance on 2024-05-03. The listed applicant is Lactation Lab, Inc.. The 510(k) number is K234088.

When did Emily's Care Nourish Test System (Model 1) receive FDA 510(k) clearance?

Emily's Care Nourish Test System (Model 1) received FDA 510(k) clearance on 2024-05-03, under 510(k) number K234088.

Who is the listed applicant for Emily's Care Nourish Test System (Model 1)?

The FDA 510(k) record lists Lactation Lab, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Emily's Care Nourish Test System (Model 1)?

The FDA product code for Emily's Care Nourish Test System (Model 1) is QEI.

Related Devices (Code: QEI)

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

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