FDA 510(k) Applications Submitted by KEN WU
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K971886 | 05/22/1997 | ACCUTEST HCG-URINE | UNOTECH DIAGNOSTICS, INC. |
| K981838 | 05/26/1998 | ACCUSTRIP HCG-URINE MODEL NUMBER HCG-002 | UNOTECH DIAGNOSTICS, INC. |
| K032987 | 09/24/2003 | ACCUTEST HCG-COMBO MODEL,HCG-004, ACCUSTRIP HCG-COMBO MODEL, HCG-005 | UNOTECH DIAGNOSTICS, INC. |
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