Intermed, Inc. - FDA 510(k) Cleared Devices
16
Total
15
Cleared
0
Denied
Intermed, Inc. has 15 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 15 cleared submissions from 1976 to 1990. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Intermed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Intermed, Inc.
16 devices
Cleared
May 22, 1990
NON STERILE PARENTERAL SUPPLY KIT
General Hospital
88d
Cleared
Feb 12, 1985
INTERMED, INS STERILE WATER/SALINE
Anesthesiology
257d
Cleared
Jan 27, 1984
DRESSING CHANGE TRAYS
General & Plastic Surgery
136d
Cleared
Jan 11, 1984
CENTRAL VEIN CATH. TRAY CC-20-1420
Cardiovascular
91d
Cleared
Jan 11, 1984
PERCUTANEOUS SHEATH INTRODUCER TRAYS
Cardiovascular
91d
Cleared
Dec 22, 1983
ACUTE HEMODIALYSIS TRAYS
Gastroenterology & Urology
99d
Cleared
Dec 12, 1983
SUCTION CATHETER TRAYS
General & Plastic Surgery
95d
Cleared
May 27, 1982
TRACHEOSTOMY CARE TRAYS
Ear, Nose, Throat
24d
Cleared
Sep 07, 1979
CATHETERIZATION TRAYS FOLEY AND URETHRAL
Gastroenterology & Urology
43d
Cleared
Aug 28, 1979
PERITONEAL PAC
Gastroenterology & Urology
33d
Cleared
Dec 12, 1978
IRRIGATION TRAY
General & Plastic Surgery
56d
Cleared
Sep 20, 1978
FOLEY CATHETERS
Gastroenterology & Urology
29d