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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