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> DevicePMAs@therightstef
PMA_Manual
Documents
(2,258)
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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
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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
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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
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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
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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
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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
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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
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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
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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
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