E. Benson Hood Laboratories, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
E. Benson Hood Laboratories, Inc. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1984 to 1999. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by E. Benson Hood Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - E. Benson Hood Laboratories, Inc.
6 devices
Cleared
Jan 29, 1999
CZAJA-MCCAFFREY RIGID STENT INTRODUCER/ENDOSCOPE
Ear, Nose, Throat
88d
Cleared
Jul 26, 1984
SALIVARY BYPASS TUBE
Gastroenterology & Urology
115d
Cleared
Jul 23, 1984
ESOPHAGEAL TUBE
Gastroenterology & Urology
112d
Cleared
Jun 14, 1984
MONTGOMERY TRACHEAL T-TUBE
Anesthesiology
80d
Cleared
May 02, 1984
LARYNGEAL STENT
Ear, Nose, Throat
30d
Cleared
May 02, 1984
UMBRELLA KEEL
Gastroenterology & Urology
30d