510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K950315Unknown

Cordis Csf Reservoir

Cordis US Corp., Miami FL / Traditional, Unknown
FDA source (opens on fda.gov)

K950315 is the FDA 510(k) clearance record for CORDIS CSF RESERVOIR, a class II device, cleared for Cordis Corp. on under FDA product code LKG (Port & Catheter, Implanted, Subcutaneous, Intraventricular). FDA records list 332 510(k) clearances for Cordis US Corp., from to . As of , FDA records show no recalls naming K950315.

Clearance record

Decision date
Received
(103 days to decision)
Product code
LKG Port & Catheter, Implanted, Subcutaneous, Intraventricular
Regulation
21 CFR 882.5550
Device class
Class II
Review panel
Neurology
Applicant
Cordis Corp. P.O. Box 025700, Miami FL
510(k) summary
Summary
Third party review
No

Clearances, product code LKG

Trailing 12 months

FDA records hold no clearances under product code LKG in the trailing twelve months.

FDA records show no clearances under product code LKG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LKG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260