Nulife
K-Number: K210969 · 2021-11-03
ApplicantMrk Healthcare Pvt, Ltd.
Decision Date2021-11-03
Product CodeKGO
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Nulife is a medical device manufactured by Mrk Healthcare Pvt, Ltd.. It received FDA 510(k) clearance on 2021-11-03 under approval number K210969. The device is classified under product code KGO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Nulife?
Nulife is a medical device that received FDA 510(k) clearance on 2021-11-03. It is manufactured by Mrk Healthcare Pvt, Ltd.. The 510(k) number is K210969.
When was Nulife approved by the FDA?
Nulife received FDA 510(k) clearance on 2021-11-03, under approval number K210969.
What company makes Nulife?
Nulife is manufactured by Mrk Healthcare Pvt, Ltd..
What is the FDA product code for Nulife?
The FDA product code for Nulife is KGO.
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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.