|
source DB |
source ID
|
text
|
size
|
updated at |
|
# proj.
|
|
# Ann.
|
updated_at |
| DevicePMAs@therightstef |
P190016_S000 |
Approval for the Tula System. This device is intended to create a myringotomy and insert a tympanos |
1.18 KB |
2020-03-03 |
|
13 |
|
0 |
-
|
| DevicePMAs@therightstef |
P180035_S000 |
Approval for MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear. This devi |
464 Bytes |
2020-03-03 |
|
13 |
|
0 |
-
|
| DevicePMAs@therightstef |
P030016_S001 |
Approval for the Visian Toric ICL (Implantable Collamer Lens). The device is indicated for use in pa |
890 Bytes |
2020-03-03 |
|
13 |
|
0 |
-
|
| DevicePMAs@therightstef |
P970032_S000 |
Approval for the SalEst(TM). This device is intended to detect and measure by enzyme-linked immunoa |
504 Bytes |
2020-03-03 |
|
13 |
|
0 |
-
|
| DevicePMAs@therightstef |
P010061_S000 |
Approval for the curelight broadband (model curelight 01). The device is indicated for use in combi |
429 Bytes |
2020-03-03 |
|
13 |
|
0 |
-
|
| DevicePMAs@therightstef |
P170027_S000 |
Approval for the TherOx Downstream System. This device is indicated for the preparation and delivery |
520 Bytes |
2020-03-03 |
|
13 |
|
0 |
-
|
| DevicePMAs@therightstef |
P940001_S000 |
This device indicated for delivering arbutamine, a catecholamine, through a closed-loop, computer-co |
1.75 KB |
2020-03-03 |
|
13 |
|
0 |
-
|
| DevicePMAs@therightstef |
P960009_S219 |
Approval to expand the indications for the Medtronic DBS system to include Epilepsy. Bilateral stimu |
837 Bytes |
2020-03-03 |
|
13 |
|
0 |
-
|
| DevicePMAs@therightstef |
P180050_S000 |
Approval for The BAROSTIM NEO System. The device is indicated for the improvement of symptoms of he |
529 Bytes |
2020-03-03 |
|
13 |
|
0 |
-
|
| DevicePMAs@therightstef |
P160048_S006 |
Approval for the Eversense CGM System. The device is indicated for continually measuring glucose le |
765 Bytes |
2020-03-03 |
|
13 |
|
0 |
-
|
