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 the device name listed in this FDA 510(k) record. The listed applicant is Front Line Medical Technologies, Inc.. It received FDA 510(k) clearance on 2021-02-22 under 510(k) 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. The listed applicant is Front Line Medical Technologies, Inc.. The 510(k) number is K201652.

When did COBRA-OS Kit receive FDA 510(k) clearance?

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

Who is the listed applicant for COBRA-OS Kit?

The FDA 510(k) record lists Front Line Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: MJN)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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.