Burron Medical Products, Inc. - FDA 510(k) Cleared Devices
41
Total
40
Cleared
0
Denied
FDA 510(k) Regulatory Record - Burron Medical Products, Inc. General Hospital ✕
23 devices
Cleared
May 01, 1987
CAVAFIX(R) CENTRAL VENOUS CATHETER KIT W/SUTURE
General Hospital
88d
Cleared
Nov 13, 1986
INTESTOPLANT
General Hospital
141d
Cleared
Jul 01, 1986
CAVAFIX, CENTRAL VENOUS CATHETER KIT
General Hospital
70d
Cleared
Jan 09, 1986
IMPLANTOFIX
General Hospital
283d
Cleared
May 01, 1984
LONG TERM CENTRAL VENOUS ACCESS CATH
General Hospital
145d
Cleared
May 01, 1984
DUAL-LUMEN LONG TERM CENTRAL VENOUS CAT
General Hospital
139d
Cleared
Apr 30, 1984
MULTI-LUMEN CENTRAL VENOUS CATH. KIT
General Hospital
132d
Cleared
Mar 24, 1983
BOTTLE ADAPTER
General Hospital
29d
Cleared
Mar 17, 1983
CLEAN-FLUSH
General Hospital
22d
Cleared
Mar 09, 1983
CAT 3040
General Hospital
48d
Cleared
Mar 08, 1982
THE INT-STOPPER
General Hospital
18d
Cleared
Mar 08, 1982
THE RED CAP
General Hospital
18d