FDA 510(k) Applications Submitted by DANIEL LEE

FDA 510(k) Number Submission Date Device Name Applicant
K970429 02/04/1997 BIOSCOPE SD TENS, ARISTA SD PLUS, AP-102080T APEX MEDICAL CORP.
K990435 02/11/1999 BESTNEB PORTABLE AEROSOL THERAPY UNIT, AP-100100 APEX MEDICAL CORP.
K002336 08/01/2000 MS104A, NEWMINI II (EMS-II), MODEL AP-101050T AND MEDTRIM (EMS-V), MODEL AP-102050T APEX MEDICAL CORP.
K002339 08/01/2000 AEMS V, EMS-1000, MODEL TS-140500 AND AEMS VI, EMS-1000 PLUS, MODEL TS-140600 APEX MEDICAL CORP.
K973978 10/20/1997 MICRO II MICROCURRENT TENS APEX MEDICAL CORP.
K973979 10/20/1997 MULTI-STIM TENS, AP-101081T APEX MEDICAL CORP.
K973980 10/20/1997 ACU-STIM TENS, AP-101082T APEX MEDICAL CORP.
K160591 03/01/2016 D.O.R.C. Disposable Cryo Probe DUTCH OPHTHALMIC RESEARCH CENTER INTERNATIONAL BV
K142877 10/01/2014 EVA,anterior machine, EVA, combined machine, EVA combined machine with laser(DORC connector), EVA combined machine with laser SMA connector) DUTCH OPHTHALMIC RESEARCH CENTER INTERNATIONAL BV


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