FDA 510(k) Premarket Notification K020558: LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE

Submission Details & Decision

Normalized public record details for 510(k) notification K020558.

Source Dataset

FDA 510(k) Premarket Notifications

510(k) Number

K020558

Applicant / Sponsor

Integra Neurosciences

Device Name

LICOX CC1.G2 BRAIN OXYGEN CATHETER-MICROPROBE

Product Code

GWM

Decision Date

2002-03-21

Decision / Status

Substantially Equivalent (SESE)

Advisory Committee

Neurology (NE)

Clearance Type

Special

Third Party Flag

Date Received

2002-02-20

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