510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K860026Substantially Equivalent

Ultramax III, Dialyzer Reprocessing Device

Medicorp, Inc., Salt Lake City UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K860026 is the FDA 510(k) clearance record for ULTRAMAX III, DIALYZER REPROCESSING DEVICE, a class II device, cleared for Medicorp, Inc. on under FDA product code LIF (Dialyzer Reprocessing System). FDA records list 5 510(k) clearances for Medicorp, Inc., from to . As of , FDA records show no recalls naming K860026.

Clearance record

Decision date
Received
(70 days to decision)
Product code
LIF Dialyzer Reprocessing System
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Medicorp, Inc. 230 W. 2950 S., Salt Lake City UT
Third party review
No

Clearances, product code LIF

Trailing 12 months

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

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