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510k Database
Manufacturers
US
Laserguide
Medical Device Manufacturer
·
US , Santa Barbara , CA
Laserguide - FDA 510(k) Cleared Devices
5 submissions
·
5 cleared
·
Since 1987
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Laserguide
General & Plastic Surgery
✕
2
devices
1-2 of 2
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Cleared
Nov 06, 1987
LIGHT-TOUCH FIBEROPTIC MICROCONTACT PROBE
K873571
·
GEX
General & Plastic Surgery
·
65d
Cleared
Nov 06, 1987
LIGHT-SPOT FIBEROPTIC LASER HANDPIECE
K873664
·
GEX
General & Plastic Surgery
·
57d
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General & Plastic Surgery
2
Gastroenterology & Urology
2
Anesthesiology
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