510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K790824Substantially Equivalent

Repgreen Ultrafiltration Monitor

Cyberex Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K790824 is the FDA 510(k) clearance record for REPGREEN ULTRAFILTRATION MONITOR, a class II device, cleared for Cyberex Corp. on under FDA product code FIL (System, Dialysate Delivery, Single Pass). FDA records list 4 510(k) clearances for Cyberex Corp., from to . As of , FDA records show no recalls naming K790824.

Clearance record

Decision date
Received
(57 days to decision)
Product code
FIL System, Dialysate Delivery, Single Pass
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Cyberex Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code FIL

Trailing 12 months

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

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