510k
Database
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1016
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4321
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3205
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2756
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464
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2325
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3927
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3591
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779
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774
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15
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1404
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1755
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857
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492
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7533
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165
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959
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4604
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1235
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LLZ
System, Image Processing,...
725
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Plate, Fixation, Bone
689
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Electrosurgical, Cutting &...
558
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System, Imaging, Pulsed Doppler,...
533
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Powered Laser Surgical Instrument
519
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Polymer Patient Examination Glove
489
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Prosthesis, Knee,...
463
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Intervertebral Fusion Device...
403
FXX
Mask, Surgical
400
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Screw, Fixation, Bone
392
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Manufacturers
US
Foley & Lardner
Medical Device Manufacturer
·
US , Washington , DC
Foley & Lardner - FDA 510(k) Cleared Devices
5 submissions
·
5 cleared
·
Since 1994
Official Website
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Foley & Lardner
Physical Medicine
✕
4
devices
1-4 of 4
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Cleared
Nov 07, 1994
DYNASTY GC 12400 (GELL/CELL)
K942308
·
KNN
Physical Medicine
·
178d
Cleared
Nov 07, 1994
DYNASTY U1-31 (GELL/CELL)
K942309
·
KNN
Physical Medicine
·
178d
Cleared
Nov 07, 1994
DYNASTY GC 12550 (GELL/CELL)
K942310
·
KNN
Physical Medicine
·
178d
Cleared
Nov 07, 1994
DYNASTY U1-33 AGM
K942311
·
KNN
Physical Medicine
·
178d
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Physical Medicine
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Cardiovascular
1