510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K260799Substantially Equivalent

Nipro Dry Acid Concentrate Mixer

Nipro Technical Solutions, Incoporated, Mesa AZ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K260799 is the FDA 510(k) clearance record for Nipro Dry Acid Concentrate Mixer, a class II device, cleared for Nipro Technical Solutions, Incoporated on under FDA product code KPO (Dialysate Concentrate For Hemodialysis (Liquid Or Powder)). As of , FDA records show no recalls naming K260799.

Clearance record

Decision date
Received
(161 days to decision)
Product code
KPO Dialysate Concentrate For Hemodialysis (Liquid Or Powder)
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Nipro Technical Solutions, Incoporated 3110 N Oakland, Suite 101, Mesa AZ
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KPO

Trailing 12 months
2 clearances under product code KPO in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KPO, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20261
September 20260
October 20260