Customed, Inc. - FDA 510(k) Cleared Devices
36
Total
26
Cleared
0
Denied
Customed, Inc. has 26 FDA 510(k) cleared medical devices. Based in Carolina Puerto Rico, US.
Historical record: 26 cleared submissions from 1990 to 1998.
Browse the FDA 510(k) cleared devices submitted by Customed, Inc. Filter by specialty or product code using the sidebar.
36 devices
Cleared
Jan 05, 1998
FANFOLD DRAPE 41 X 57 PRODUCT NO. 900-633, RECORDER NO. 0633
General Hospital
24d
Cleared
Dec 04, 1997
GOWN POLY REINFORCED LARGE(PRODUCT NO.900-522)/(REORDER NO. 0522)
General Hospital
195d
Cleared
Nov 25, 1996
SUCTION CATHETER TRAY PRODUCT NO. 900277
General & Plastic Surgery
49d
Cleared
Oct 04, 1996
URINARY DRAINAGE BAG, (REORDER NO. 0749 - PRODUCT NO. 900-749)
Gastroenterology & Urology
88d
Cleared
Sep 27, 1996
CUSTOMED BLOOD EXTRACTION KIT
Chemistry
87d
Cleared
May 09, 1996
UNIVERSAL DRAINAGE TRAY
Gastroenterology & Urology
24d
Cleared
Oct 02, 1995
STERIMED STERIZATION WRAPPER (NON-STERILE)
General Hospital
56d
Cleared
Apr 18, 1995
WOUND CLOSURE/LACERATION TRAY
General & Plastic Surgery
84d
Cleared
Sep 08, 1994
FOLEY CATHETERIZATION TRAY
Gastroenterology & Urology
127d
Cleared
Aug 27, 1993
IV PREP KIT (NON-STERILE)
General & Plastic Surgery
337d
Cleared
Aug 27, 1993
IV PREP KIT W/O DRESSING (NON-STERILE)
General & Plastic Surgery
337d
Cleared
Jul 14, 1993
BLOOD GAS KIT (NON-STERILE) REORDER NO. 0560
Anesthesiology
139d