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 a medical device manufactured by Curio Digital Therapeutics, Inc.. It received FDA 510(k) clearance on 2024-04-22 under approval 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. It is manufactured by Curio Digital Therapeutics, Inc.. The 510(k) number is K223515.
When was MamaLift Plus approved by the FDA?
MamaLift Plus received FDA 510(k) clearance on 2024-04-22, under approval number K223515.
What company makes MamaLift Plus?
MamaLift Plus is manufactured by Curio Digital Therapeutics, Inc..
What is the FDA product code for MamaLift Plus?
The FDA product code for MamaLift Plus is SAP.
Related Devices (Code: SAP)
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.