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> DevicePMAs@therightstef
Age_blah
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DevicePMAs@therightstef
P930014_S084
Approval to modify the acrysert c delivery system by reducing the size of the nozzle tip, adding an external nozzle tip depth guard, and adding a plunger spring and plunger lock, the device, as modifi
566 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P090022_S004
Approval to extend the power range for which lenses are marketed in 1/4 diopter increment from 18.0 through 25.0 diopters to 15.0 through 25.0 diopters. The device, as modified, will be marketed unde
467 Bytes
2020-03-03
11
4
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DevicePMAs@therightstef
P080004_S007
Approval for packaging changes to the model py-60ad. The device, as modified, will be marketed under the trade name isert model py-60adc and is indicated for primary implantation in the capsular bag
310 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P880091_S010
Approval for lens model aa-4207vf. The device is to be placed in the capsular bag of the eye and is indicated for primary implantation for the visual correction of aphakia in persons 60 years of age
315 Bytes
2020-03-03
11
4
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DevicePMAs@therightstef
P980040_S065
Approval for the Tecnis Symfony Extended Range of Vision Intraocular Lens. The TECNIS Symfony Extended Range of Vision IOL, Model ZXR00, is indicated for primary implantation for the visual correctio
1.3 KB
2020-03-03
11
0
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DevicePMAs@therightstef
P990013_S014
Approval for parametric lot release using existing validated steam sterilization cycles. The device, as modified, will be marketed under the trade name collamer ultraviolet-absorbing posterior chambe
546 Bytes
2020-03-03
11
4
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DevicePMAs@therightstef
P870073_S017
Approval to modify the directions for use for all legally marketed iols under the referenced pmas, to indicate the iols for use in adult patients. Previously, the iols were indicated for use in perso
484 Bytes
2020-03-03
11
2
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DevicePMAs@therightstef
P090022_S022
Approval to reduce the size of the secondary packaging which houses the pouched intraocular lenses, label and directions for use (dfu). the device, as modified, will be marketed under the trade name s
376 Bytes
2020-03-03
11
4
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DevicePMAs@therightstef
P060022_S000
Approval for the akreos posterior chamber intraocular lens (iol), model: akreos advanced optics aspheric lens, ao60. The device is indicated for primary implantation for the visual correction of apha
344 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P010027_S000
Approval for the allergan, inc. model ac21b ultraviolet-absorbing pmma anterior chamber intraocular lens, available in three overall diameters (12.0 mm, 13.0 mm, 14.0 mm). The application is a licens
1.03 KB
2020-03-03
11
4
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