510k
Database
Specialties
Anesthesiology
204
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740
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187
Dental
470
Ear, Nose, Throat
92
Gastroenterology & Urology
397
General & Plastic Surgery
777
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476
Hematology
77
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64
Medical Genetics
1
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277
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304
Obstetrics & Gynecology
118
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79
Orthopedic
1478
Pathology
26
Physical Medicine
153
Radiology
1097
Toxicology
94
Categories
IYN
System, Imaging, Pulsed Doppler,...
167
HRS
Plate, Fixation, Bone
151
OLO
Orthopedic Stereotaxic Instrument
131
GEX
Powered Laser Surgical Instrument
127
LLZ
System, Image Processing,...
125
QIH
Automated Radiological Image...
113
GEI
Electrosurgical, Cutting &...
105
NHA
Abutment, Implant, Dental,...
105
MAX
Intervertebral Fusion Device...
96
NKB
Thoracolumbosacral Pedicle Screw...
93
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Allergan, Inc.
Medical Device Manufacturer
·
US , Walker , MI
Allergan, Inc. - FDA 510(k) Cleared Devices
33 submissions
·
33 cleared
·
Since 1982
Official Website
33
Total
33
Cleared
0
Denied
FDA 510(k) cleared devices by Allergan, Inc.
Neurology
✕
1
devices
1-1 of 1
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Cleared
Sep 14, 2005
SINGLE AMPLIFIER FOR BOTOX
K051852
·
GWL
Neurology
·
68d
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33
Ophthalmic
29
General & Plastic Surgery
2
Neurology
1
Dental
1