FDA 510(k) Applications Submitted by CASE MEDICAL, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K991023 03/29/1999 STERITITE PERFORATED BOTTOM RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02 - POLYPROPYLENE NON-WOVEN DISPOSABL CASE MEDICAL, INC.
K974638 10/10/1997 STERITITE SEALED CONTAINERS MODEL SCO4Q CASE MEDICAL, INC.
K030853 03/18/2003 STERITITE PERFORATED BASE RIGID REUSABLE STERILIZATION CONTAINER SYSTEM WITH SCF02-POLYPROPYLENE NON-WOVEN DISPOSABLE FI CASE MEDICAL, INC.
K982151 06/18/1998 STERITITE PROCESS INDICATOR ACCESSORIES CASE MEDICAL, INC.
K022978 09/06/2002 STERITITE CONTAINER WITH FLASHTITE VALVE PLATE(S) & MEDITRAY PRODUCTS CASE MEDICAL, INC.
K023614 10/28/2002 STERITITE RIGID REUSABLE STERILIZATION CONTAINER SYSTEM CASE MEDICAL, INC.
K221492 05/23/2022 SteriTite Container System with MediTray Parts Case Medical, Inc.
K212711 08/26/2021 SteriTite Container System with MediTray Products Case Medical, Inc.
K090068 01/09/2009 STERITITE UNIVERSAL CONTAINER SYSTEM AND MEDITRAY PRODUCTS CASE MEDICAL, INC.
K080558 02/28/2008 STERITITE CONTAINER SYSTEM & MEDITRAY PRODUCTS CASE MEDICAL, INC.
K110682 03/10/2011 STERITITE CONTAINER SYSTEM & MEDITRAY PRODUCTS CASE MEDICAL, INC.
K161415 05/23/2016 SteriTite Containers System & MediTray Products CASE MEDICAL, INC.
K112904 10/04/2011 STERITEC CONTAINERS SYSTEM & MEDITRAY PRODUCTS CASE MEDICAL, INC.


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