|
source DB |
source ID
|
text
|
size
|
updated at |
|
# proj.
|
|
# Ann.
|
updated_at |
| DevicePMAs@therightstef |
P040039_S000 |
Approval for the orbasone pain relief system. The device is indicated for extracorporeal shock wave |
443 Bytes |
2020-03-03 |
|
13 |
|
4 |
-
|
| DevicePMAs@therightstef |
P080028_S000 |
Approval for the storz medical duolith sd1 shock wave therapy. this device is indicated for extracor |
500 Bytes |
2020-03-03 |
|
13 |
|
4 |
-
|
| DevicePMAs@therightstef |
P990055_S001 |
Approval for the addition of the assay to the bayer acs: 180 and advia centaur analyzers. The devic |
634 Bytes |
2020-03-03 |
|
13 |
|
4 |
-
|
| DevicePMAs@therightstef |
P980031_S000 |
This device is indicated for the reduction or elimination of mild myopia (-2.00 to -3.00 diopters sp |
404 Bytes |
2020-03-03 |
|
13 |
|
4 |
-
|
| DevicePMAs@therightstef |
P990052_S015 |
Approval for a change in the wording of the indications for use statement and a new product code des |
402 Bytes |
2020-03-03 |
|
13 |
|
5 |
-
|
| DevicePMAs@therightstef |
P110039_S000 |
Approval for the exablate system, model 2000/2100 /2100 vi. this device is indicated for pain pallia |
419 Bytes |
2020-03-03 |
|
13 |
|
4 |
-
|
| DevicePMAs@therightstef |
P990078_S000 |
Approval for the sunrise hyperion(tm) ltk system. The device is indicated for temporary reduction o |
500 Bytes |
2020-03-03 |
|
13 |
|
4 |
-
|
| DevicePMAs@therightstef |
P920030_S002 |
Approval for the addition of a new indication for use. The device, as modified, will be marketed un |
485 Bytes |
2020-03-03 |
|
13 |
|
4 |
-
|
| DevicePMAs@therightstef |
P850048_S017 |
Approval for the access hybritech psa on the access 2 immunoassay analyzer. The device is indicated |
704 Bytes |
2020-03-03 |
|
13 |
|
4 |
-
|
| DevicePMAs@therightstef |
P100044_S000 |
Approval for the propel sinus implant. This device is indicated for use in patients >= 18 years of |
430 Bytes |
2020-03-03 |
|
13 |
|
4 |
-
|
