Tillotson Rubber Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tillotson Rubber Co., Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Tillotson Rubber Co., Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1977 to 1991. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tillotson Rubber Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tillotson Rubber Co., Inc.
6 devices
Cleared
Feb 25, 1991
PILGRIM NITRILE LATEX GLOVES (VARIOUS TYPES)
General Hospital
60d
Cleared
Sep 05, 1990
STERILE PATIENT EXAMINATION GLOVES
General Hospital
23d
Cleared
Aug 17, 1990
POWDER FREE, NON-STERILE EXAMINATION GLOVES
General Hospital
10d
Cleared
May 07, 1990
HPI ORTHO SURGEONS' GLOVE
General Hospital
280d
Cleared
Feb 21, 1978
GLOVES, FLOOR
General Hospital
18d
Cleared
Jun 24, 1977
GLOVES, SURGEONS, LATEX
General Hospital
67d