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Thd Spa

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
13
Inspections
0
Compliance Actions
1

Recent 510(k) Clearances

K-NumberDeviceDate
K211623THD Procto Software SystemJune 24, 2021
K193512THD Procto Software SystemJanuary 26, 2020
K180135THD Anopress with THD SensyProbeMarch 8, 2018
K161785THD ANOPRESSMarch 14, 2017
K141657THD REVOLUTIONFebruary 24, 2015
K133687THD N-ANO ANOSCOPEDecember 11, 2013
K121135THD ANOSCOPE, PROCTOSCOPE, RECTOSCOPE, RECTOSCOPE AND LIGHT-SCOPEJune 1, 2012
K103647THD DISPOSABLE ANOSCOPES, PROCTOSCOPES AND RECTOSCOPESMarch 1, 2011
K093497THD BANDYJuly 15, 2010
K091490FAMILY OF THD DISPOSABLE ANOSCOPES/PROCTOSCOPES/RECTOSCOPESJune 11, 2009
K090009THD SLIDE ONEJanuary 28, 2009
K081429THD SLIDEJuly 30, 2008
K080132THD DISPOSABLE ANOSCOPE/PROCTOSCOPEApril 9, 2008