Medi-Ject Corp. is one of 21653 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medi-Ject Corp. - FDA 510(k) Cleared Devices
Recent clearances: MODIFICATION TO MEDI-JECT CORPORATION MEDI-JECTOR CHOICE NEEDLE-FREE INSULIN DELIVERY SYSTEM, MEDI-JECTOR CHOICE NEEDLE-FREE INSULIN DELIVERY SYSTEM, MEDI-JECT CORPORATION MEDI-JECTOR NEEDLE-FREE BIO-TROPIN DDRUG DELIVERY SYSTEMS 0.0058/0.0068(INCH DIAMETER NOZZLEORIFIC
3
Total
3
Cleared
0
Denied
Medi-Ject Corp. has 3 FDA 510(k) cleared medical devices. Based in Minneapolis, US.
Historical record: 3 cleared submissions from 1996 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medi-Ject Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medi-Ject Corp.
3 devices
Cleared
Apr 23, 1999
MODIFICATION TO MEDI-JECT CORPORATION MEDI-JECTOR CHOICE NEEDLE-FREE INSULIN...
General Hospital
8d
Cleared
Oct 07, 1996
MEDI-JECTOR CHOICE NEEDLE-FREE INSULIN DELIVERY SYSTEM
General Hospital
69d
Cleared
Apr 17, 1996
MEDI-JECT CORPORATION MEDI-JECTOR NEEDLE-FREE BIO-TROPIN DDRUG DELIVERY...
General Hospital
89d