CORDIS CSF RESERVOIR— 510(k) K950315

Unknown

Cordis Corp.

FDA 510(k) clearance K950315 for CORDIS CSF RESERVOIR, Unknown on 1995-05-09. Applicant: Cordis Corp.. Device class: 2.

Clearance details

Applicant
Cordis Corp.
Product code
Code LKG
Device class
Class 2
Regulation
21 CFR 882.5550
Advisory panel
Neurology
Date received
Decision date
Decision
Unknown
Clearance type
Traditional
Location
Miami, FL, US
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