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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
Gastroenterology & Urology
✕
2
devices
1-2 of 2
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Cleared
Mar 22, 1988
SURGI-LIGHT ND:YAG LASER FOR UROLOGICAL USE
K880071
·
FCS
Gastroenterology & Urology
·
71d
Cleared
Feb 02, 1988
SURGI-LIGHT DISPOS.FIBEROPTIC DEL/SYS GI/URO USE
K873892
·
LNK
Gastroenterology & Urology
·
132d
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General & Plastic Surgery
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