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 the device name listed in this FDA 510(k) record. The listed applicant is Neonatal Loving Kare, Inc.. It received FDA 510(k) clearance on 2018-01-18 under 510(k) 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. The listed applicant is Neonatal Loving Kare, Inc.. The 510(k) number is K172962.
When did Nurture Rest receive FDA 510(k) clearance?
Nurture Rest received FDA 510(k) clearance on 2018-01-18, under 510(k) number K172962.
Who is the listed applicant for Nurture Rest?
The FDA 510(k) record lists Neonatal Loving Kare, Inc. as the applicant. This does not by itself establish the device manufacturer.
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.