Multi-Med, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Multi-Med, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Multi-Med, Inc. has 7 FDA 510(k) cleared medical devices. Based in West Swanzey, US.
Historical record: 7 cleared submissions from 1989 to 1989. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Multi-Med, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Multi-Med, Inc.
7 devices
Cleared
Jun 14, 1989
ENTERAL FEEDING CONTAINER
Gastroenterology & Urology
139d
Cleared
May 23, 1989
EXTERNAL FEEDING SET FOR PUMP USE
Gastroenterology & Urology
119d
Cleared
May 18, 1989
INJECTION SITE PLUG (INTRAVASCULAR ADMINISTRATION)
General Hospital
73d
Cleared
May 05, 1989
INTRAVASCULAR ADMINISTRATION SET
General Hospital
39d
Cleared
Apr 21, 1989
INTRAVASCULAR ADMINISTRATION SET
General Hospital
51d
Cleared
Mar 31, 1989
INTRAVASCULAR ADMINISTRATION SET
General Hospital
67d
Cleared
Feb 03, 1989
INTRAVASCULAR ADMINISTRATION SET
General Hospital
22d