Aplicare, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aplicare, Inc. - FDA 510(k) Cleared Devices
9
Total
9
Cleared
0
Denied
Aplicare, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 9 cleared submissions from 1983 to 1994. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Aplicare, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Aplicare, Inc.
9 devices
Cleared
Jan 18, 1994
APLICARE ONE COMPUND BENZION TINCTURE SWABSTICK
General & Plastic Surgery
561d
Cleared
Oct 03, 1989
STERILE SALINE - FOR SUCTION CATHETER LUBRICATION
General Hospital
55d
Cleared
Nov 23, 1987
APLICARE STERILE WATER - FOR SUCTION CATHETER ONLY
General Hospital
82d
Cleared
Jul 11, 1986
APLICARE SKIN PROTECTANT PREP PAD
General & Plastic Surgery
77d
Cleared
Jun 04, 1986
APLICARE SKIN PROTECTANT SWABSTICK
General & Plastic Surgery
40d
Cleared
Oct 31, 1983
APLICARE ONE ACETONE ALCOHOL SWABSTICK
General Hospital
42d
Cleared
Oct 31, 1983
ACETONE ALCOHOL PREP PAD
General Hospital
42d
Cleared
Oct 27, 1983
APLICARE ALCOHOL PREP PAD
General Hospital
38d
Cleared
Oct 27, 1983
APLICARE THREE ALCOHOL SWABSTICKS
General Hospital
38d