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)

Cor-Knot Micro

K-Number: K202551 · 2021-06-24

Decision Date2021-06-24
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Cor-Knot Micro is a medical device manufactured by Lsi Solutions, Inc.. It received FDA 510(k) clearance on 2021-06-24 under approval 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. It is manufactured by Lsi Solutions, Inc.. The 510(k) number is K202551.

When was Cor-Knot Micro approved by the FDA?

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

What company makes Cor-Knot Micro?

Cor-Knot Micro is manufactured by Lsi Solutions, Inc..

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

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

Other Devices by Lsi Solutions, Inc.

Related Devices (Code: GCJ)

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.