Medical Device Manufacturer · IT , S. Lazzaro Di Savena, Bologna

Thd Spa - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2008
13
Total
13
Cleared
0
Denied

FDA 510(k) cleared devices by Thd Spa Gastroenterology & Urology ✕

8 devices
1-8 of 8
Cleared Mar 08, 2018
THD Anopress with THD SensyProbe
K180135 · KLA
Gastroenterology & Urology · 50d
Cleared Mar 14, 2017
THD ANOPRESS
K161785 · KLA
Gastroenterology & Urology · 258d
Cleared Dec 11, 2013
THD N-ANO ANOSCOPE
K133687 · FER
Gastroenterology & Urology · 9d
Cleared Jun 01, 2012
THD ANOSCOPE, PROCTOSCOPE, RECTOSCOPE, RECTOSCOPE AND LIGHT-SCOPE
K121135 · FER
Gastroenterology & Urology · 49d
Cleared Mar 01, 2011
THD DISPOSABLE ANOSCOPES, PROCTOSCOPES AND RECTOSCOPES
K103647 · FER
Gastroenterology & Urology · 78d
Cleared Jul 15, 2010
THD BANDY
K093497 · FHN
Gastroenterology & Urology · 245d
Cleared Jun 11, 2009
FAMILY OF THD DISPOSABLE ANOSCOPES/PROCTOSCOPES/RECTOSCOPES
K091490 · FER
Gastroenterology & Urology · 22d
Cleared Apr 09, 2008
THD DISPOSABLE ANOSCOPE/PROCTOSCOPE
K080132 · FER
Gastroenterology & Urology · 82d
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