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Documents
(3,322)
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# proj.
# Ann.
updated_at
DevicePMAs@therightstef
P010015_S016
Approval for modifications to the device labeling to describe the care-hf clinical study. medtronic
904 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P960040_S053
Approval for the vitality he model t180 implantable cardioverter defibrillator (icd) system and the
373 Bytes
2020-03-03
11
0
-
DevicePMAs@therightstef
P960040_S025
Approval for vitality automatic implantable cardioverter defibrillator (aicd) systems (vitality dr m
791 Bytes
2020-03-03
11
0
-
DevicePMAs@therightstef
P090013_S281
Approval for an update to the indications for use to include pacing at the bundle of His. The device
459 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P090013_S124
Approval for software changes to the mycarelink patient monitor m2.5 model 24950 with model 24955 rf
349 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P090013_S200
Approval of the evera mri xt/s dr and vr implantable cardioverterdefibrillator devices and programme
825 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P010012_S165
Approval for the teligen implantable cardioverter defibrillator models e102 and e110, the cognis car
1006 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P960040_S155
Approval for the teligen implantable cardioverter defibrillator models e102 and e110, the cognis car
1006 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P010012_S255
Approval for incepta, energen. punctua and teligen icd models and the incepta, energen. punctua and
854 Bytes
2020-03-03
11
0
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DevicePMAs@therightstef
P960040_S036
Approval for changes to the indications for use and clinical study section labeling. The devices ar
1.24 KB
2020-03-03
9
0
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