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510k Database
Manufacturers
US
Endotek Corp.
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Medical Device Manufacturer
·
US , Walker , MI
Endotek Corp. - FDA 510(k) Cleared Devices
2 submissions
·
2 cleared
·
Since 1980
View 2 510(k) Devices ↓
2
Total
2
Cleared
0
Denied
FDA 510(k) Regulatory Record - Endotek Corp.
Gastroenterology & Urology
✕
2
devices
1-2 of 2
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Cleared
Aug 08, 1984
EMG MODULE, EMG1, W/OPTIONAL SPEAKER
K842124
·
FAP
Gastroenterology & Urology
·
71d
Cleared
Nov 24, 1980
ROBERTSON OBTURATION MONITOR INSUFFLA
K802374
·
FAP
Gastroenterology & Urology
·
56d
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Gastroenterology & Urology
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