FDA 510(k) Applications Submitted by VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB

FDA 510(k) Number	Submission Date	Device Name	Applicant
K000618	02/17/2000	SCANDINAVIAN IVF SCIENCES AB, THAW-KIT 1	VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
K000619	02/17/2000	SCANDINAVIAN IVF SCIENCES AB, G2.2	VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
K000621	02/17/2000	SCANDINAVIAN IVF SCIENCES AB, SPERMRINSE -20/100	VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
K000626	02/17/2000	SCANDINAVIAN IVF SCIENCES AB, GAMETE-100	VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
K000627	02/17/2000	SCANDINAVIAN IVF SCIENCES AB, HYBASE-1	VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
K000623	02/17/2000	SCANDINAVIAN IVF SCIENCES AB, FREEZE-KIT 1	VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB
K000625	02/17/2000	SCANDINAVIAN IVF SCIENCES AB, G1.2	VITROLIFE AB/SCANDINAVIAN IVF SCIENCES AB