National Custom Ent., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
National Custom Ent., Inc. - FDA 510(k) Cleared Devices
12
Total
11
Cleared
0
Denied
National Custom Ent., Inc. has 11 FDA 510(k) cleared medical devices. Based in Burnsville, US.
Historical record: 11 cleared submissions from 1993 to 2001. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by National Custom Ent., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - National Custom Ent., Inc.
12 devices
Cleared
Oct 10, 2001
MARQUETTE EAGLE MONITOR MODEL 4000, MODEL N3024
Cardiovascular
84d
Cleared
Oct 10, 2001
MARQUETTE MAC8, MAC PERSONAL, MAC STRESS, MODEL N3043IWC
Cardiovascular
84d
Cleared
Sep 12, 2001
MEDFUSION 2001 & 2010, MODEL N7215IWC
General Hospital
56d
Cleared
Sep 12, 2001
BAXTER AS40A, AS41 SYRINGE PUMP, MODEL N61WC
General Hospital
56d
Cleared
Sep 12, 2001
SHERWOOD 224, 324 FEEDING PUMP & K524 INTRI-FLUSH, MODEL N7213IWC2
General Hospital
56d
Cleared
Sep 10, 2001
SCALE-TRONIX 48, 2001, 2009,2700,3003,4004, 4800,...
General Hospital
56d
Cleared
Nov 04, 1994
REPLACEMENT BATTERIES
Gastroenterology & Urology
101d
Cleared
Nov 04, 1994
NCE REPLACEMENT BATTERIES
Gastroenterology & Urology
101d
Cleared
Aug 18, 1994
NCE REPLACEMENT BATTERIES
Cardiovascular
76d
Cleared
Jul 26, 1994
NCE REPLACEMENT BATTERIES
Cardiovascular
92d
Cleared
Jun 24, 1994
REPLACEMENT BATTERIES/WELCH ALLYN #72200 POWER HANDLE
Ear, Nose, Throat
87d
Cleared
Oct 07, 1993
POWRPAK REPLACEMENT BATTERIES FOR PHISIO-CONTROL LIFEPAK 5/10
Cardiovascular
48d