510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K823092Substantially Equivalent

Hemaflo Blood Tubing Sets

Cobe Laboratories, Inc., Walker MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K823092 is the FDA 510(k) clearance record for HEMAFLO BLOOD TUBING SETS, a class II device, cleared for Cobe Laboratories, Inc. on under FDA product code FKQ (System, Dialysate Delivery, Central Multiple Patient). FDA records list 77 510(k) clearances for Cobe Laboratories, Inc., from to . As of , FDA records show no recalls naming K823092.

Clearance record

Decision date
Received
(33 days to decision)
Product code
FKQ System, Dialysate Delivery, Central Multiple Patient
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Cobe Laboratories, Inc. 4221 Richmond Rd., NW, Walker MI
Third party review
No

Clearances, product code FKQ

Trailing 12 months

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

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