The Medi-Dose Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Medi-Dose Group - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
The Medi-Dose Group has 10 FDA 510(k) cleared general hospital devices. Based in Feasterville, US.
Historical record: 10 cleared submissions from 1989 to 1995.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - The Medi-Dose Group
10 devices
Cleared
Sep 15, 1995
TRANSFEER SPIKE II
General Hospital
126d
Cleared
Oct 07, 1994
1.2 MICRON AIR ELIMINATING FILTER
General Hospital
127d
Cleared
May 07, 1990
TS-1800 MEDICATION TRANSFER SPIKE
General Hospital
87d
Cleared
Dec 27, 1989
CHEMO-SPIKE RECONSTITUTION DEVICE
General Hospital
124d
Cleared
Dec 27, 1989
IV DISPESNSING SPIKE
General Hospital
124d
Cleared
Dec 01, 1989
INJECTION PORT II --- FOR INTERMITTENT INJECTION
General Hospital
31d
Cleared
Nov 24, 1989
DISPOSABLE DISC FILTER
General Hospital
84d
Cleared
Jul 25, 1989
INJECTION PORT FOR---INTERMITTENT INJECTION
General Hospital
106d
Cleared
Jul 14, 1989
COMBI-CAP
General Hospital
95d
Cleared
Jul 14, 1989
DISPOSABLE DISC FILTER
General Hospital
95d