FDA 510(k) Applications Submitted by PETER WEI
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K994118 |
12/06/1999 |
OSMANTHUS, KONGFU, AND GOBON, NATURAL RUBBER LATEX CONDOMS |
GUILIN LATEX FACTORY |
| K021775 |
05/29/2002 |
LTFS230 |
HEALTHTRONICS, INC. |
| K012785 |
08/20/2001 |
TWINTRODE ELC 134 ELECTRODE |
HEALTH TRONICS SURGICAL SERVICES, INC. |
| K000963 |
03/24/2000 |
DA VINCHI EEG AND EMG/EP SYSTEMS |
AIRSEP CORP. |
| K001013 |
03/29/2000 |
MONET ACQUISITION SYSTEM FOR EEG AND POLYSOMNOGRAPHY |
AIRSEP CORP. |
| K150930 |
04/06/2015 |
Deployable Oxygen Generation System-Smaill (DOGS-S) |
AirSep Corporation |
| K101154 |
04/23/2010 |
CENTROX, RELIANT, ULTROX, AS-D+, AS-E, AS-G, AS-J, AS-K AND AS-L |
AIRSEP CORP. |
| K001467 |
05/10/2000 |
DA VINCHI EMG/EP ISA1004EP |
AIRSEP CORP. |
| K080348 |
02/11/2008 |
OXISCAN II DATA MANAGEMENT SYSTEM |
AIRSEP CORP. |
|
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