FDA 510(k)

LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE

K-Number: K020558 · 2002-03-21

Decision Date2002-03-21

Product CodeGWM

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE is the device name listed in this FDA 510(k) record. The listed applicant is Integra Neurosciences. It received FDA 510(k) clearance on 2002-03-21 under 510(k) number K020558. The device is classified under product code GWM. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE?

LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE is a medical device that received FDA 510(k) clearance on 2002-03-21. The listed applicant is Integra Neurosciences. The 510(k) number is K020558.

When did LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE receive FDA 510(k) clearance?

LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE received FDA 510(k) clearance on 2002-03-21, under 510(k) number K020558.

Who is the listed applicant for LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE?

The FDA 510(k) record lists Integra Neurosciences as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE?

The FDA product code for LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE is GWM.

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Related Devices (Code: GWM)

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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.