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FDA 510(k)

MamaLift Plus

K-Number: K223515 · 2024-04-22

ApplicantCurio Digital Therapeutics, Inc.
Decision Date2024-04-22
Product CodeSAP
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MamaLift Plus is the device name listed in this FDA 510(k) record. The listed applicant is Curio Digital Therapeutics, Inc.. It received FDA 510(k) clearance on 2024-04-22 under 510(k) number K223515. The device is classified under product code SAP. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MamaLift Plus?

MamaLift Plus is a medical device that received FDA 510(k) clearance on 2024-04-22. The listed applicant is Curio Digital Therapeutics, Inc.. The 510(k) number is K223515.

When did MamaLift Plus receive FDA 510(k) clearance?

MamaLift Plus received FDA 510(k) clearance on 2024-04-22, under 510(k) number K223515.

Who is the listed applicant for MamaLift Plus?

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

What is the FDA product code for MamaLift Plus?

The FDA product code for MamaLift Plus is SAP.

Related Devices (Code: SAP)

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.

K254038Motivista (CT-155)Click Therapeutics, Inc.K231209RejoynOtsuka America Pharmaceutical, Inc.

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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