Medi-Dose, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medi-Dose, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Medi-Dose, Inc. has 4 FDA 510(k) cleared medical devices. Based in Feasterville, US.
Historical record: 4 cleared submissions from 1994 to 1998. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medi-Dose, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medi-Dose, Inc.
4 devices
Cleared
Jan 08, 1998
CHEMO-SPIKE II RECONSTITUTION DEVICE
General Hospital
45d
Cleared
Jul 28, 1995
SAFE CAP NEEDLE RECAPPING/UNCAPPING DEVICE
General Hospital
102d
Cleared
Dec 12, 1994
DISPOSABLE DISC FILTER
General Hospital
361d
Cleared
Aug 17, 1994
2 MICRON AIR ELIMINATING FILTER
General Hospital
82d