FDA 510(k) Applications Submitted by DAVID SLAVIN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K080073 |
01/11/2008 |
S-TEST CREATININE (CRE) |
ALFA WASSERMANN, INC. |
| K072140 |
08/02/2007 |
S40 CLINICAL ANALYZER, S TEST BIL, S TEST BUN, S TEST GLU |
ALFA WASSERMANN DIAGNOSTIC TECHNOLOGIES, INC. |
| K072141 |
08/02/2007 |
S40 CLINICAL ANALYZER, S TEST IP, S TEST UA |
ALFA WASSERMANN DIAGNOSTIC TECHNOLOGIES, INC. |
| K072142 |
08/02/2007 |
S40 CLINICAL ANALYZER, S TEST ALP, S TEST AMYLASE, S TEST AST |
ALFA WASSERMANN DIAGNOSTIC TECHNOLOGIES, INC. |
| K072143 |
08/02/2007 |
S40 CLINICAL ANALYZER, S TEST ALB |
ALFA WASSERMANN DIAGNOSTIC TECHNOLOGIES, INC. |
| K072356 |
08/22/2007 |
S-TEST CA |
ALFA WASSERMANN DIAGNOSTIC TECHNOLOGIES, INC. |
| K073223 |
11/15/2007 |
S-TEST C02 |
ALFA WASSERMANN DIAGNOSTIC TECHNOLOGIES, INC. |
| K003558 |
11/17/2000 |
TCI COMBI (TINNITUS CONTROL INSTRUMENT COMBINATION) |
SIEMENS HEARING INSTRUMENTS, INC. |
| K003559 |
11/17/2000 |
TCI (TINNITUS CONTROL INSTRUMENT) |
SIEMENS HEARING INSTRUMENTS, INC. |
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