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FDA 510(k)

Cor-Knot Micro

K-Number: K202551 · 2021-06-24

ApplicantLsi Solutions, Inc.
Decision Date2021-06-24
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Cor-Knot Micro is the device name listed in this FDA 510(k) record. The listed applicant is Lsi Solutions, Inc.. It received FDA 510(k) clearance on 2021-06-24 under 510(k) number K202551. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Cor-Knot Micro?

Cor-Knot Micro is a medical device that received FDA 510(k) clearance on 2021-06-24. The listed applicant is Lsi Solutions, Inc.. The 510(k) number is K202551.

When did Cor-Knot Micro receive FDA 510(k) clearance?

Cor-Knot Micro received FDA 510(k) clearance on 2021-06-24, under 510(k) number K202551.

Who is the listed applicant for Cor-Knot Micro?

The FDA 510(k) record lists Lsi Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Cor-Knot Micro?

The FDA product code for Cor-Knot Micro is GCJ.

Other records listing Lsi Solutions, Inc. as applicant

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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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