510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K820695Substantially Equivalent

Automatic Dialyzer Reprocessor #Adr-22

Texas Medical Devices, Inc., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K820695 is the FDA 510(k) clearance record for AUTOMATIC DIALYZER REPROCESSOR #ADR-22, a class II device, cleared for Texas Medical Devices, Inc. on under FDA product code LIF (Dialyzer Reprocessing System). FDA records list one 510(k) clearance for Texas Medical Devices, Inc. As of , FDA records show no recalls naming K820695.

Clearance record

Decision date
Received
(48 days to decision)
Product code
LIF Dialyzer Reprocessing System
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Texas Medical Devices, Inc. 803 N. Front St. Suite 3, Mchenry IL
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