Sheridan Catheter Corp. - FDA 510(k) Cleared Devices
39
Total
39
Cleared
0
Denied
Sheridan Catheter Corp. has 39 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 39 cleared submissions from 1982 to 1993. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Sheridan Catheter Corp. Filter by specialty or product code using the sidebar.
39 devices
Cleared
May 07, 1993
LAZER-TRACH TRACHEAL TUBE
Anesthesiology
325d
Cleared
Mar 23, 1990
LASER RESISTANT TRACHEAL TUBE
Anesthesiology
95d
Cleared
May 05, 1989
ACCESSORY TO CLINICAL ELECTRONIC THERMOMETER
General Hospital
77d
Cleared
Feb 16, 1989
CLINICAL ELECTRONIC THERMOMETERS
General Hospital
94d
Cleared
Dec 05, 1988
KIM NASO-INTESTINAL TUBE
Gastroenterology & Urology
146d
Cleared
Aug 04, 1988
CLINICAL ELECTRONIC THERMOMETERS
General Hospital
76d
Cleared
Jul 13, 1988
CLINICAL ELECTONIC THERMOMETERS
General Hospital
22d
Cleared
Jun 16, 1988
SHERIDAN ELECTROSURGERY PROTECTION FILTER
Anesthesiology
80d
Cleared
May 18, 1988
INTRODUCTION/DRAINAGE CATHETER & ACCESS
General & Plastic Surgery
15d
Cleared
Apr 29, 1988
NDYAG LASER TRACHEAL TUBE
Anesthesiology
52d
Cleared
Jan 19, 1988
ESOPHAGEAL OBTURATOR/TRACHEAL TUBE
Anesthesiology
28d
Cleared
Nov 24, 1987
ESOPHAGEAL STETHOSCOPE W/ELECTRICAL CONDUCTORS
Anesthesiology
35d
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