510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K992255Substantially Equivalent

Ckhemo, Model Ckhemo Version 1.0

Csam, Inc., Bettendorf IA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K992255 is the FDA 510(k) clearance record for CKHEMO, MODEL CKHEMO VERSION 1.0, a class II device, cleared for Csam, Inc. on under FDA product code FKP (System, Dialysate Delivery, Single Patient). FDA records list one 510(k) clearance for Csam, Inc. As of , FDA records show no recalls naming K992255.

Clearance record

Decision date
Received
(147 days to decision)
Product code
FKP System, Dialysate Delivery, Single Patient
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Csam, Inc. 1890 14th St., Bettendorf IA
510(k) summary
Statement
Third party review
No

Clearances, product code FKP

Trailing 12 months

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

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