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FDA 510(k)

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 the device name listed in this FDA 510(k) record. The listed applicant is Mrk Healthcare Pvt, Ltd.. It received FDA 510(k) clearance on 2021-11-03 under 510(k) 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. The listed applicant is Mrk Healthcare Pvt, Ltd.. The 510(k) number is K210969.

When did Nulife receive FDA 510(k) clearance?

Nulife received FDA 510(k) clearance on 2021-11-03, under 510(k) number K210969.

Who is the listed applicant for Nulife?

The FDA 510(k) record lists Mrk Healthcare Pvt, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Nulife?

The FDA product code for Nulife is KGO.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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