510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K003023Substantially Equivalent

Cobe Hc 700 Midi Hemoconcentrator

Hospal Industrie, Arvada CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K003023 is the FDA 510(k) clearance record for COBE HC 700 MIDI HEMOCONCENTRATOR, a class II device, cleared for Hospal Industrie on under FDA product code KDI (Dialyzer, High Permeability With Or Without Sealed Dialysate System). FDA records list one 510(k) clearance for Hospal Industrie. As of , FDA records show no recalls naming K003023.

Clearance record

Decision date
Received
(214 days to decision)
Product code
KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System
Regulation
21 CFR 876.5860
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Hospal Industrie 14401 W. 65th Way, Arvada CO
510(k) summary
Summary
Third party review
No

Clearances, product code KDI

Trailing 12 months
6 clearances under product code KDI in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code KDI, trailing twelve months
MonthClearances
November 20250
December 20251
January 20261
February 20261
March 20261
April 20260
May 20261
June 20260
July 20261
August 20260
September 20260
October 20260