FDA 510(k) Applications Submitted by Roger De Bock
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K130275 | 02/04/2013 | QUIKSCREEN MULTI (MDMA AND OPI) OTC DRUG CUP TEST | Tianjin New Bay Bioresearch Co., Ltd. |
| K122064 | 07/13/2012 | FORSURE ONE STEP BUPRENORPHINE CUP TEST DEVICE | Tianjin New Bay Bioresearch Co., Ltd. |
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