510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K800991Substantially Equivalent

Cordia N

Cordis US Corp., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K800991 is the FDA 510(k) clearance record for CORDIA N, a class II device, cleared for Cordis Corp. on under FDA product code DHC (System, Test, Systemic Lupus Erythematosus). FDA records list 332 510(k) clearances for Cordis US Corp., from to . As of , FDA records show no recalls naming K800991.

Clearance record

Decision date
Received
(14 days to decision)
Product code
DHC System, Test, Systemic Lupus Erythematosus
Regulation
21 CFR 866.5820
Device class
Class II
Review panel
Immunology
Applicant
Cordis Corp. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code DHC

Trailing 12 months

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

FDA records show no clearances under product code DHC in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code DHC, 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