Tillotson Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Tillotson Corp. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Tillotson Corp. has 4 FDA 510(k) cleared medical devices. Based in Everett, US.
Historical record: 4 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Tillotson Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Tillotson Corp.
4 devices
Cleared
Jul 14, 1989
NON STERILE EXAM GLOVES ( TILLOTSON RUBBER CO.)
General Hospital
108d
Cleared
Jul 14, 1989
PATIENT EXAM GLOVES (MFG. MOSS POINT GLOVE CO.)
General Hospital
108d
Cleared
Jul 14, 1989
LATEX EXAMINATION GLOVES
General Hospital
45d
Cleared
Jun 22, 1989
HPI NON STERILE EXAM GLOVES
General Hospital
71d