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Search FDA 510(k) devices
510k Database
Manufacturers
US
Laser Media
Medical Device Manufacturer
·
US , Hauppauge , NY
Laser Media - FDA 510(k) Cleared Devices
12 submissions
·
12 cleared
·
Since 1985
12
Total
12
Cleared
0
Denied
FDA 510(k) Regulatory Record - Laser Media
Anesthesiology
✕
2
devices
1-2 of 2
Filters
Cleared
Dec 11, 1987
FIBERLASE II ND:YAG LASER FOR PULMONARY USE
K872351
·
LLO
Anesthesiology
·
177d
Cleared
Jan 14, 1985
FIBERLASE 100 MEDICAL LASER SYSTEM
K844869
·
LLO
Anesthesiology
·
31d
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