510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K113869Substantially Equivalent

Origen Reinforced Dual Lumen Catheter

OriGen Biomedical, Inc., Austin TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K113869 is the FDA 510(k) clearance record for ORIGEN REINFORCED DUAL LUMEN CATHETER, a class II device, cleared for Origen Biomedical, Inc. on under FDA product code DWF (Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass). FDA records list 4 510(k) clearances for Origen Biomedical, Inc., from to . As of , FDA records show 16 recalls naming K113869.

Clearance record

Decision date
Received
(209 days to decision)
Product code
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Regulation
21 CFR 870.4210
Device class
Class II
Review panel
Cardiovascular
Applicant
Origen Biomedical, Inc. 7000 Burleson Rd. Bldg. D, Austin TX
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DWF

Trailing 12 months
6 clearances under product code DWF in the twelve months to October 2026, January 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code DWF, trailing twelve months
MonthClearances
November 20250
December 20250
January 20262
February 20262
March 20261
April 20261
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260