FDA 510(k) Applications Submitted by WYNTEK DIAGNOSTICS, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K990576 |
02/23/1999 |
OSOM CARD PREGNANCY TEST, MODEL 103 |
WYNTEK DIAGNOSTICS, INC. |
K990578 |
02/23/1999 |
OSOM CARD II HCG-URINE TEST, MODEL 102 |
WYNTEK DIAGNOSTICS, INC. |
K961423 |
04/12/1996 |
OSOM STREP A TEST |
WYNTEK DIAGNOSTICS, INC. |
K972231 |
06/16/1997 |
OSOM MONO TEST 143 |
WYNTEK DIAGNOSTICS, INC. |
K992658 |
08/09/1999 |
OSOM ULTRA STREP A TEST, MODEL 147 |
WYNTEK DIAGNOSTICS, INC. |
K973879 |
09/10/1997 |
OSOM CARD HCG-URINE TEST |
WYNTEK DIAGNOSTICS, INC. |
K974159 |
10/14/1997 |
OSOM HCG-URINE TEST MODEL 101 |
WYNTEK DIAGNOSTICS, INC. |
K965184 |
12/24/1996 |
PERFECTA PREGNANCY TEST |
WYNTEK DIAGNOSTICS, INC. |
K965227 |
12/30/1996 |
OSOM CLASSIC HCG-URINE TEST (115) |
WYNTEK DIAGNOSTICS, INC. |
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