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510k Database
Manufacturers
US
Regtec
Medical Device Manufacturer
·
US , St. Petersburg , FL
Regtec - FDA 510(k) Cleared Devices
1 submissions
·
1 cleared
·
Since 1986
1
Total
1
Cleared
0
Denied
FDA 510(k) Regulatory Record - Regtec
Gastroenterology & Urology
✕
1
devices
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Cleared
Feb 19, 1986
FRITCH OPHTHALMIC ENDOSCOPE
K855151
·
GDB
Gastroenterology & Urology
·
55d
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Gastroenterology & Urology
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