Life-Tech, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
14
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K120234EZONO 3000April 19, 2012
K111355ECHOBRIGHTSeptember 16, 2011
K102813EZONO 3000June 30, 2011
K102007PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,December 22, 2010
K093662ECHOBRIGHTJune 24, 2010
K093485VESISCANMarch 16, 2010
K082772STIMPRO, MODELS SP22050, SP20100, SPP19050, SPP19100, SPP19150, SPC19050, SPC19100, SPC19150, SPC180February 9, 2009
K082056ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1November 7, 2008
K082923PRLONG, MODELS PL50, PL100, PL-40C, PL-50C, PL-100C, PL-150C, PLT-40C, PLT-50C, PLT-100C, PLT-150COctober 24, 2008
K081864PROLONGSeptember 25, 2008
K073187PERIPHERAL NERVE BLOCK SUPPORT TRAYApril 22, 2008
K072050PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CSOctober 18, 2007
K052954CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SETFebruary 15, 2006
K050499PROBLOC, HN SERIES AND PROLONG, PL SERIESMay 17, 2005