Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Nurture Rest

K-Number: K172962 · 2018-01-18

ApplicantNeonatal Loving Kare, Inc.
Decision Date2018-01-18
Product CodeOUW
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

Nurture Rest is a medical device manufactured by Neonatal Loving Kare, Inc.. It received FDA 510(k) clearance on 2018-01-18 under approval number K172962. The device is classified under product code OUW. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Nurture Rest?

Nurture Rest is a medical device that received FDA 510(k) clearance on 2018-01-18. It is manufactured by Neonatal Loving Kare, Inc.. The 510(k) number is K172962.

When was Nurture Rest approved by the FDA?

Nurture Rest received FDA 510(k) clearance on 2018-01-18, under approval number K172962.

What company makes Nurture Rest?

Nurture Rest is manufactured by Neonatal Loving Kare, Inc..

What is the FDA product code for Nurture Rest?

The FDA product code for Nurture Rest is OUW.

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.

↑