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FDA 510(k)

COBRA-OS Kit

K-Number: K201652 · 2021-02-22

ApplicantFront Line Medical Technologies, Inc.
Decision Date2021-02-22
Product CodeMJN
Advisory CommitteeCV
DecisionUnknown

Device Summary

COBRA-OS Kit is a medical device manufactured by Front Line Medical Technologies, Inc.. It received FDA 510(k) clearance on 2021-02-22 under approval number K201652. The device is classified under product code MJN. It was reviewed by the CV advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the COBRA-OS Kit?

COBRA-OS Kit is a medical device that received FDA 510(k) clearance on 2021-02-22. It is manufactured by Front Line Medical Technologies, Inc.. The 510(k) number is K201652.

When was COBRA-OS Kit approved by the FDA?

COBRA-OS Kit received FDA 510(k) clearance on 2021-02-22, under approval number K201652.

What company makes COBRA-OS Kit?

COBRA-OS Kit is manufactured by Front Line Medical Technologies, Inc..

What is the FDA product code for COBRA-OS Kit?

The FDA product code for COBRA-OS Kit is MJN.

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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.

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