Life-Tech, Inc.
Life-Tech, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2012.
Top product codes for Life-Tech, Inc.
Recent clearances by Life-Tech, Inc.
- K120234 — EZONO 3000
- K111355 — ECHOBRIGHT
- K102813 — EZONO 3000
- K102007 — PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,
- K093662 — ECHOBRIGHT
- K093485 — VESISCAN
- K082772 — STIMPRO, MODELS SP22050, SP20100, SPP19050, SPP19100, SPP19150, SPC19050, SPC19100, SPC19150, SPC18050,SPC18100,SPC18150
- K082056 — ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1
- K082923 — PRLONG, MODELS PL50, PL100, PL-40C, PL-50C, PL-100C, PL-150C, PLT-40C, PLT-50C, PLT-100C, PLT-150C
- K081864 — PROLONG
- K073187 — PERIPHERAL NERVE BLOCK SUPPORT TRAY
- K072050 — PROLONG-EX, MODELS: PLEX-50CS, PLEX-100CS, PLEX-150CS
- K052954 — CONTISTIM CONTINUOUS STIMULATING CATHETER NERVE BLOCK SET
- K050499 — PROBLOC, HN SERIES AND PROLONG, PL SERIES
Data sourced from openFDA. This site is unofficial and independent of the FDA.